8-[3-amino-piperidin-1-yl]-xanthines, the production thereof and the use of the same as medicaments

0001The present invention relates to novel substituted xanthines of the general formula<chemistry id="chem0001" num="0001"><img file="EP1532149B1_D0001.tif" /></chemistry>their tautomers, enantiomers, diastereomers, their mixtures and their salts, in particular their physiologically acceptable salts with inorganic or organic acids or bases, which have valuable pharmacological properties, in particular an inhibitory effect on the activity of the enzyme dipeptidyl peptidase-IV (DPP-IV), the Manufacture, their use for the prevention or treatment of diseases or conditions associated with increased DPP-IV activity or which can be prevented or alleviated by reduction of DPP-IV activity, in particular diabetes mellitus type I or type II, the a compound of the general formula (I) or a physiologically acceptable salt thereof containing medicament and process for their preparation.

0002In the above formula I mean R¹ a 4-methoxy-1-naphthylmethyl group, a 2-quinolinylmethyl, 4-quinolinylmethyl or a 6-quinolinylmethyl group, a 1-isoquinolinylmethyl, 3-methyl-1-isoquinolinylmethyl, 4-methyl-1-isoquinolinylmethyl or a 3-isoquinolinylmethyl group or a 2-quinazolinylmethyl, 4-methyl-2-quinazolinylmethyl or a 4-quinazolinylmethyl group, R² a methyl group and R³ a 2-buten-1-yl or a 2-butin-1-yl group, their tautomers, enantiomers, diastereomers, their mixtures and their salts.

0003Very particular preference is given to the following compounds of the general formula I:<ol id="ol0001"><li>(1) 1 - [(quinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - ((<i>R</i>) -3-amino-piperidin-1-yl) -xanthine,</li><li>(2) 1 - [(3-methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - ((<i>S</i>) -3-aminopiperidine-1-yl) -xanthine,</li><li>(3) 1 - [(3-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - ((<i>R</i>) -3-aminopiperidine-1-yl) -xanthine,</li><li>(4) 1 - [(4-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - ((<i>S</i>) -3-aminopiperidine-1-yl) -xanthine,</li><li>(5) 1 - [(4-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - ((<i>R</i>) -3-aminopiperidine-1-yl) -xanthine,</li><li>(6) 1 - [(4-methoxynaphthalen-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - ((<i>S</i>) -3-aminopiperidine-1-yl) -xanthine,</li><li>(7) 1 - [(4-methoxynaphthalen-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - ((<i>R</i>) -3-aminopiperidine-1-yl) -xanthine,</li><li>(8) 1 - [(4-Methylquinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- (3- (3)<i>R</i>) Aminopiperidine-1-yl) -xanthine,</li></ol>and their tautomers, enantiomers, diastereomers, their mixtures and their salts.

0004According to the invention, the compounds of general formula I are obtained by processes known per se, for example by the following processes:<ol id="ol0002" compact="compact"><li>a) reaction of a compound of the general formula<chemistry id="chem0002" num="0002"><img file="EP1532149B1_D0002.tif" /></chemistry>in the<ul id="ul0001" list-style="none" compact="compact"><li>R¹ to R³ as defined above are defined and</li><li>Z¹ a leaving group such as a halogen atom, a substituted hydroxy, mercapto, sulfinyl, sulfonyl or sulfonyloxy group such as a chlorine or bromine atom, a methanesulfonyl or methanesulfonyloxy group, with 3-aminopiperidine, its enantiomers or its salts.</li></ul>The reaction is conveniently carried out in a solvent such as isopropanol, butanol, tetrahydrofuran, dioxane, dimethylformamide, dimethyl sulfoxide, ethylene-glycol monomethyl ether, ethylene glycol diethyl ether or sulfolane optionally in the presence of an inorganic or tertiary organic base, eg sodium carbonate, potassium carbonate or potassium hydroxide, a tertiary organic base, eg Triethylamine, or in the presence of N-ethyl-diisopropylamine (Hünig base), these organic bases can also serve as a solvent at the same time, and optionally in the presence of a reaction accelerator such as an alkali metal halide or a palladium-based catalyst at temperatures between -20 and 180 ° C, but preferably at temperatures between -10 and 120 ° C performed.However, the reaction can also be carried out without a solvent or in an excess of 3-aminopiperidine.</li><li>b) Deprotection of a compound of the general formula<chemistry id="chem0003" num="0003"><img file="EP1532149B1_D0003.tif" /></chemistry>in the R¹, R² and R³ as defined above.</li></ol>

0005The cleavage of the tert-Butyloxycarbonylrestes is preferably carried out by treatment with an acid such as trifluoroacetic acid or hydrochloric acid or by treatment with bromotrimethylsilane or iodotrimethylsilane optionally using a solvent such as methylene chloride, ethyl acetate, dioxane, methanol, isopropanol or diethyl ether at temperatures between 0 and 80 ° C. ,

0006In the reactions described above, optionally present reactive groups such as carboxy, amino, alkylamino or imino groups can be protected during the reaction by conventional protecting groups, which are cleaved again after the reaction.

0007For example, protective groups for a carboxy group include the trimethylsilyl, methyl, ethyl, tert-butyl, benzyl or tetrahydropyranyl group, as protecting groups for an amino, alkylamino or imino group, the formyl, acetyl, trifluoroacetyl, ethoxycarbonyl -, tert-butoxycarbonyl, benzyloxycarbonyl, benzyl, methoxybenzyl or 2,4-dimethoxybenzyl and for the amino group additionally the phthalyl group into consideration.

0008The optional subsequent cleavage of a protective moiety used is carried out, for example hydrolytically in an aqueous solvent, for example in water, isopropanol / water, acetic acid / water, tetrahydrofuran / water or dioxane / water, in the presence of an acid such as trifluoroacetic acid, hydrochloric acid or sulfuric acid or in the presence of an alkali metal base such as sodium hydroxide or potassium hydroxide or aprotic, for example in the presence of iodotrimethylsilane, at temperatures between 0 and 120 ° C, preferably at temperatures between 10 and 100 ° C.

0009However, the cleavage of a benzyl, methoxybenzyl or Benzyloxycarbonylrestes example, hydrogenolytically, for example with hydrogen in the presence of a catalyst such as palladium / carbon in a suitable solvent such as methanol, ethanol, ethyl acetate or glacial acetic acid, optionally with the addition of an acid such as hydrochloric acid at temperatures between 0 and 100 ° C, but preferably at room temperatures between 20 and 60 ° C, and at a hydrogen pressure of 1 to 7 bar, but preferably from 3 to 5 bar. However, the cleavage of a 2,4-dimethoxybenzyl radical is preferably carried out in trifluoroacetic acid in the presence of anisole.

0010The elimination of a tert-butyl or tert-Butyloxycarbonylrestes is preferably carried out by treatment with an acid such as trifluoroacetic acid or hydrochloric acid or by treatment with iodotrimethylsilane optionally with the use of a solvent such as methylene chloride, dioxane, methanol or diethyl ether.

0011The cleavage of a Trifluoracetylrestes is preferably carried out by treatment with an acid such as hydrochloric acid optionally in the presence of a solvent such as acetic acid at temperatures between 50 and 120 ° C or by treatment with sodium hydroxide, optionally in the presence of a solvent such as tetrahydrofuran at temperatures between 0 and 50 ° C.

0012The cleavage of a Phthalylrestes preferably takes place in the presence of hydrazine or a primary amine such as methylamine, ethylamine or n-butylamine in a solvent such as methanol, ethanol, isopropanol, toluene / water or dioxane at temperatures between 20 and 50 ° C.

0013Furthermore, as already mentioned, the compounds of general formula I obtained can be separated into their enantiomers and / or diastereomers. Thus, for example, cis / trans mixtures can be separated into their cis and trans isomers, and compounds having at least one optically active carbon atom can be separated into their enantiomers.

0014Thus, for example, the cis- / trans mixtures obtained can be purified by chromatography into their cis- and trans-isomers, the compounds of general formula I which are obtained in racemates, by methods known per se (see <nplcit id="ncit0001" npl-type="b"><text>Allinger NL and Eliel EL in "Topics in Stereochemistry", Vol. 6, Wiley Interscience, 1971</text></nplcit>) in their optical antipodes and compounds of general formula I with at least 2 asymmetric carbon atoms due to their physicochemical differences according to known methods, for example by chromatography and / or fractional crystallization, in their diastereomers, which, if they are in racemic form can then be separated into the enantiomers as mentioned above.

0015The enantiomer separation is preferably carried out by column separation on chiral phases or by recrystallization from an optically active solvent or by reacting with a, with the racemic compound salts or derivatives such as esters or amides forming optically active substance, in particular acids and their activated derivatives or alcohols, and Separation of the thus obtained diastereomeric salt mixture or derivative, for example due to different solubilities, wherein from the pure diastereomeric salts or derivatives, the free antipodes can be released by the action of suitable agents. Particularly common, optically active acids are, for example, the D and L forms of tartaric acid or dibenzoyltartaric acid, di-Op-toluoyl-tartaric acid, malic acid, mandelic acid, camphorsulfonic acid, glutamic acid, Aspartic or quinic acid. Examples of optically active alcohols are (+) - or (-) - menthol and, for example, (+) - or (-) - menthyloxycarbonyl as the optically active acyl radical in amides.

0016Furthermore, the resulting compounds of the formula I can be converted into their salts, in particular for the pharmaceutical application in their physiologically acceptable salts with inorganic or organic acids. Examples of suitable acids are hydrochloric acid, hydrobromic acid, sulfuric acid, methanesulfonic acid, phosphoric acid, fumaric acid, succinic acid, lactic acid, citric acid, tartaric acid or maleic acid.

0017The compounds of the general formulas II to III used as starting materials are either known from the literature or are obtained by processes known per se from the literature (see Examples I to LXXI).

0018As already mentioned, the compounds of the general formula I according to the invention and their physiologically tolerated salts have valuable pharmacological properties, in particular an inhibiting action on the enzyme DPP-IV.

0019The biological properties of the new compounds were tested as follows:

0020The ability of the substances and their corresponding salts to inhibit DPP-IV activity can be demonstrated in an experimental setup using an extract of the human colon carcinoma cell line Caco-2 as a DPP-IV source. Differentiation of cells to induce DPP-IV expression was performed as described by Reiher et al. in an article entitled "<nplcit id="ncit0002" npl-type="s"><text>Increased expression of intestinal cell line Caco-2 ", published in Proc. Natl. Acad Sci., Vol. 90, pages 5757-5761 (1993</text></nplcit>), carried out. The cell extract was purified from cells solubilized in a buffer (10mM Tris HCl, 0.15M NaCl, 0.04% aprotinin, 0.5% Nonidet-P40, pH 8.0) by centrifugation at 35,000g for 30 minutes at 4 ° C (to remove cell debris). won.

0021The DPP-IV assay was performed as follows:

002250 μl of substrate solution (AFC, amido-4-trifluoromethylcoumarin AFC), final concentration 100 μM, were placed in black microtiter plates. 20 μl assay buffer (final concentrations 50 mM Tris HCl pH 7.8, 50 mM NaCl, 1% DMSO) was pipetted. The reaction was started by adding 30 μl solubilized Caco-2 protein (final concentration 0.14 μg protein per well). The test substances to be tested were typically added prediluted in 20 μl, with the assay buffer volume correspondingly reduced. The reaction was carried out at room temperature, the incubation time was 60 minutes. The fluorescence was then measured in a Victor 1420 Multilabel Counter with the excitation wavelength at 405 nm and the emission wavelength at 535 nm. Blank values ​​(corresponding to 0% activity) were obtained in batches without Caco-2 protein (volume replaced by assay buffer), control values ​​(corresponding to 100% activity) were obtained in batches without added substance. The potency of the respective test substances, expressed as IC₅₀ Values ​​were calculated from dose-response curves consisting of 11 measurement points each. The following results were obtained:<tables id="tabl0001" num="0001"><table frame="all"><tgroup cols="2"><colspec colnum="1" colname="col1" colwidth="39mm" /><colspec colnum="2" colname="col2" colwidth="45mm" /><thead><row><entry align="center" valign="top">Connection (example no.)</entry><entry align="center" valign="top">DPP IV inhibition IC₅₀ [NM]</entry></row></thead><tbody><row rowsep="0"><entry align="center">2 (52)</entry><entry align="center">9</entry></row><row rowsep="0"><entry align="center">2 (80)</entry><entry align="center">1</entry></row><row rowsep="0"><entry align="center">2 (129)</entry><entry align="center">3</entry></row><row rowsep="0"><entry align="center">2 (130)</entry><entry align="center">3</entry></row><row rowsep="0"><entry align="center">2 (131)</entry><entry align="center">3</entry></row><row rowsep="0"><entry align="center">2 (132)</entry><entry align="center">1</entry></row><row rowsep="0"><entry align="center">2 (137)</entry><entry align="center">13</entry></row><row rowsep="0"><entry align="center">2 (138)</entry><entry align="center">8th</entry></row><row><entry align="center">2 (142)</entry><entry align="center">1</entry></row></tbody></tgroup></table></tables>

0023The compounds prepared according to the invention are well tolerated since, for example, no changes in the behavior of the animals could be observed after oral administration of 10 mg / kg of the compound of Example 2 (80) to rats.

0024In view of the ability to inhibit DPP-IV activity, the compounds of general formula I according to the invention and their corresponding pharmaceutically acceptable salts are capable of affecting all those conditions or diseases which may be affected by inhibition of DPP-IV activity , It is therefore expected that the compounds of the invention will be useful in the prevention or treatment of diseases or conditions such as Type 1 and Type 2 diabetes mellitus, diabetic complications (such as retinopathy, nephropathy or neuropathies), metabolic acidosis or ketosis, reactive hypoglycemia, insulin resistance, metabolic Syndrome, dyslipidemias of various genesis, arthritis, atherosclerosis and related diseases, obesity, Allograft transplantation and calcitonin-induced osteoporosis. In addition, these substances are suitable for preventing B cell degeneration such as apoptosis or necrosis of pancreatic B cells. The substances are further suited to improve or restore the functionality of pancreatic cells, in addition to increase the number and size of pancreatic B cells. In addition, and due to the role of glucagon-like peptides such as GLP-1 and GLP-2 and their linkage with DPP-IV inhibition, it is expected that the compounds of the present invention will be useful for, inter alia, achieving a sedative or anxiolytic effect . In addition, catabolic states after surgery or hormonal stress responses can be favorably influenced or the mortality and morbidity after myocardial infarction can be reduced. Moreover, they are suitable for treating all conditions related to the above-mentioned effects mediated by GLP-1 or GLP-2. The compounds of the invention are also useful as diuretics or antihypertensives and are suitable for the prevention and treatment of acute renal failure. Furthermore, the compounds according to the invention can be used for the treatment of inflammatory diseases of the respiratory tract. Likewise, they are suitable for the prevention and treatment of chronic inflammatory bowel diseases such as irritable bowel syndrome (IBS), Crohn's disease or ulcerative colitis as well as in pancreatitis. Furthermore, it is expected that they can be used in any kind of injury or impairment in the gastrointestinal tract as well as in colitis and enterids. Moreover, it is expected that DPP-IV inhibitors, and thus also the compounds of the present invention, can be used to treat infertility or improve human or mammalian fertility, particularly if infertility is associated with insulin resistance or polycystic ovarian syndrome , On the other hand, these substances are suitable for influencing the motility of the sperm and thus can be used as contraceptives for use in men. Furthermore, the substances are suitable for influencing growth hormone deficiencies associated with short stature, and in all indications where growth hormone can be used. The compounds of the invention are due to their inhibitory effect against DPP IV also suitable for the treatment of various autoimmune diseases such as rheumatoid arthritis, multiple sclerosis, thyroiditis and Basedow's disease etc .. Moreover, they can be used in viral diseases as well as eg in HIV infections, for the stimulation of blood formation, for benign prostatic hyperplasia, for gingivitis, as well as for the treatment of neuronal defects and neurodegenerative diseases such as Alzheimer's disease. Described compounds are also to be used for the therapy of tumors, in particular for the modification of tumor invasion as well as metastatization, Examples include T cell lymphoma, acute lymphoblastic leukemia, cell-based thyroid carcinoma, basal cell carcinoma or breast carcinoma. Other indications include stroke, ischemia of various origins, Parkinson's disease and migraine. In addition, other indications are follicular and epidermal hyperkeratosis, increased keratinocyte proliferation, psoriasis, encephalomyelitis, glomerulonephritides, lipodystrophies, as well as psychosomatic, depressive and neuropsychiatric disorders of various origins.

0025The compounds according to the invention can also be used in combination with other active substances. Therapeutics suitable for such a combination include, for example, antidiabetic agents such as metformin, sulfonylureas (eg, glibenclamide, tolbutamide, glimepiride), nateglinides, repaglinide, thiazolidinediones (eg, rosiglitazone, pioglitazone), PPAR-gamma agonists (eg, GI 262570), and Antagonists, PPAR-gamma / alpha modulators (eg KRP 297), alpha-glucosidase inhibitors (eg acarbose, voglibose), other DPP-IV inhibitors, alpha2-antagonists, insulin and insulin analogs, GLP-1 and GLP-1 analogues (eg exendin) 4) or amylin. In addition, SGLT2 inhibitors such as T-1095, inhibitors of protein tyrosine phosphatase 1, substances that influence a deregulated production of glucose in the liver, such as inhibitors of glucose-6-phosphatase,₃Agonists such as SB-418790 or AD-9677 as well as agonists of the 5HT2c receptor.

0026In addition, a combination with drugs for influencing the hypertension such as all antagonists or ACE inhibitors, diuretics, β-blockers, Ca antagonists and others, or combinations thereof is suitable.

0027The dosage required to achieve a corresponding effect is expediently when intravenously administered 1 to 100 mg, preferably 1 to 30 mg, and when administered orally 1 to 1000 mg, preferably 1 to 100 mg, in each case 1 to 4 times daily. For this purpose, the compounds of the formula I according to the invention, optionally in combination with other active substances, together with one or more inert customary carriers and / or diluents, for example with corn starch, lactose, cane sugar, microcrystalline cellulose, magnesium stearate, polyvinylpyrrolidone, citric acid, tartaric acid, Water, water / ethanol, water / glycerol, water / sorbitol, water / polyethylene glycol, propylene glycol, cetylstearyl alcohol, carboxymethyl cellulose or fatty substances such as hard fat or their suitable mixtures,

0028The following examples are intended to explain the invention in more detail:

Preparation of the starting compounds:

Example I

1,3-dimethyl-7- (2,6-dicyano-benzyl)

<u>-</u>

8-bromo-xanthine

0029A mixture of 555 mg of 8-Bromtheophyllin and 0.39 ml Hünigbase in 9 ml of N, N-dimethylformamide is mixed with 600 mg of 2-bromomethyl-isophthalonitrile and stirred overnight at room temperature. For workup, the reaction mixture is poured onto water. The precipitate is filtered off, washed with water and dried. Yield: 686 mg (83% of theory) R_fValue: 0.56 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 399, 401 [M + H]⁺

0030Analogously to Example I, the following compounds are obtained:<ol id="ol0003"><li>(1) 3-Methyl-7- (3-methyl-2-buten-1-yl) -8-chloro-xanthine Mass Spectrum (ESI⁺): m / z = 269, 271 [M + H]⁺</li><li>(2) 3-methyl-7- (2-cyano-benzyl) -8-chloro-xanthine Mass Spectrum (ESI⁺): m / z = 316, 318 [M + H]⁺</li><li>(3) 1- (2-Phenyl-2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8-bromo-xanthine Mass Spectrum (ESI⁺): m / z = 415, 417 [M + H]⁺</li><li>(4) 3-methyl-7 - [(2-trimethylsilanylethoxy) methyl] -8-bromo-xanthine (carried out in the presence of potassium carbonate) Mass Spectrum (ESI⁺): m / z = 375, 377 [M + H]⁺</li><li>(5) 3-Methyl-7- (3-methyl-2-buten-1-yl) -8-bromo-xanthine Mass Spectrum (ESI⁺): m / z = 313, 315 [M + H]⁺</li><li>(6) 3-Methyl-7- (2,3-dimethyl-2-buten-1-yl) -8-bromo-xanthine R_fValue: 0.43 (silica gel, methylene chloride / methanol = 9: 1) Mass Spectrum (ESI⁺): m / z = 327, 329 [M + H]⁺</li><li>(7) 3-Methyl-7- (2-butyn-1-yl) -8-bromo-xanthine R_fValue: 0.72 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 297/299 [M + H]⁺</li><li>(8) 3-Methyl-7 - ((E) -2-buten-1-yl) -8-bromo-xanthine (The product is contaminated with approx. 10-20% Z compound) R_fValue: 0.55 (silica gel, cyclohexane / ethyl acetate / methanol = 6: 3: 1) mass spectrum (ESI⁺): m / z = 299, 301 [M + H]⁺</li><li>(9) 3-Methyl-7 - [(1-cyclopenten-1-yl) methyl] -8-bromo-xanthine Mass Spectrum (ESI⁺): m / z = 325, 327 [M + H]⁺</li><li>(10) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7 - [(1-cyclopenten-1-yl) methyl] -8-bromo-xanthine Mass Spectrum (ESI⁺): m / z = 443, 445 [M + H]⁺</li><li>(11) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7 - ((E) -2-buten-1-yl) -8-bromo-xanthine (Product contains about 25% Z-isomer) Mass Spectrum (ESI⁺): m / z = 417, 419 [M + H]⁺</li><li>(12) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7- (2-methyl-allyl) -8-bromo-xanthine R_fValue: 0.71 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 417, 419 [M + H]⁺</li><li>(13) 1- (2-Phenyl-2-oxo-ethyl) -3-methyl-7- (3-bromo-allyl) -8-bromo-xanthine R_fValue: 0.68 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 481, 483, 485 [M + H]⁺</li><li>(14) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7 - [(furan-2-yl) methyl] -8-bromo-xanthine R_fValue: 0.60 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 443, 445 [M + H]⁺</li><li>(15) 1- (2-Phenyl-2-oxo-ethyl) -3-methyl-7- (2-chloro-allyl) -8-bromo-xanthine R_fValue: 0.77 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 437, 439, 441 [M + H]⁺</li><li>(16) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7 - ((Z) -2-methyl-2-buten-1-yl) -8-bromo-xanthine R_fValue: 0.77 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 431, 433 [M + H]⁺</li><li>(17) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7 - ((E) -2-methyl-2-buten-1-yl) -8-bromo-xanthine R_fValue: 0.77 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 431, 433 [M + H]⁺</li><li>(18) 1- (2-Phenyl-2-oxo-ethyl) -3-methyl-7- (1-phenylsulfanyl-butyl) -8-bromo-xanthine R_fValue: 0.83 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 527, 529 [M + H]⁺</li><li>(19) 3-Methyl-7- (3-methyl-1-phenylsulfanyl-butyl) -8-bromo-xanthine (The [(1-chloro-3-methylbutyl) sulfanyl] benzene used as starting material for the reaction is obtained by chlorinating [(3-methylbutyl) sulfanyl] benzene with N-chloro-succinimide in carbon tetrachloride). R_fValue: 0.38 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 423, 425 [M + H]⁺</li><li>(20) 1,3-Dimethyl-7- (2-bromobenzyl) -8-chloro-xanthine R_fValue: 0.50 (silica gel, cyclohexane / ethyl acetate = 1: 1)</li><li>(21) 1,3-Dimethyl-7- (2-chloro-benzyl) -8-chloro-xanthine R_fValue: 0.50 (silica gel, cyclohexane / ethyl acetate = 1: 1)</li><li>(22) 3-Cyclopropyl-7- (2-butyn-1-yl) -8-bromo-xanthine R_fValue: 0.45 (reversed phase DC precast plate (E. Merck), acetonitrile / water / trifluoroacetic acid = 50: 50: 1) Mass Spectrum (ESI⁺): m / z = 223/225 [M + H]⁺</li></ol>

Example II

1- (2- {2 - [(ethoxycarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine

0031To a mixture of 200 mg of 1- [2- (2-hydroxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3 - (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine and 63 mg of potassium carbonate in 3 ml of N, N-dimethylformamide are added 63 mg of ethyl bromoacetate. The reaction mixture is stirred for five hours at room temperature. For workup, it is mixed with water and the precipitate is filtered off, washed with water and dried for three hours at 80 ° C in a drying oven. Yield: 216 mg (94% of theory) Mass Spectrum (ESI⁺): m / z = 653 [M + H]⁺

0032The following compounds are obtained analogously to Example II:<ol id="ol0004"><li>(1) 1- (2- {2 - [(Aminocarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 624 [M + H]⁺</li><li>(2) 1- (2- {3 - [(Methylsulfanyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_f-ert: 0.20 (silica gel, cyclohexane / ethyl acetate = 6: 4) Mass Spectrum (ESI⁺): m / z = 627 [M + H]⁺</li><li>(3) 1- (2- {3 - [(ethoxycarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.50 (silica gel, cyclohexane / ethyl acetate = 3: 7)</li><li>(4) 1- (2- {2 - [(Methylaminocarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 638 [M + H]⁺</li><li>(5) 1- (2- {2 - [(Dimethylaminocarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 652 [M + H]⁺</li><li>(6) 1- (2- {3 - [(Methoxycarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 639 [M + H]⁺</li><li>(7) 1- (2- {2 - [(ethylaminocarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 636 [M + H]⁺</li><li>(8) 1- (2- {2 - [(Methylaminocarbonyl) methoxy] phenyl} -2-oxo-ethyl) -3-methyl-7 - [(1-cyclopenten-1-yl) methyl] -8- [ 3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 650 [M + H]⁺</li><li>(9) 1- (2- {2 - [(Methylaminocarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8- [3- ( tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 622 [M + H]⁺</li><li>(10) 1- (2- {2 - [(Aminocarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8- [3- ( tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 608 [M + H]⁺</li><li>(11) 1- (2- {2 - [(Methoxycarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8- [3- ( tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 623 [M + H]⁺</li><li>(12) 1- (2- {2 - [(isopropyloxycarbonyl) methoxy] phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 667 [M + H]⁺</li><li>(13) 1- (2- {2 - [(Methylaminocarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 622 [M + H]⁺</li><li>(14) 1- (2- {2 - [(Methylaminocarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7 - ((E) -2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Product contains some Z-isomer) R_fValue: 0.35 (silica gel, cyclohexane / ethyl acetate / methanol = 5: 4: 1) Mass Spectrum (ESI⁺): m / z = 624 [M + H]⁺</li><li>(15) 1- (2- {2 - [(ethylaminocarbonyl) methoxy] phenyl} -2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 636 [M + H]⁺</li><li>(16) 1- (2- {2 - [(Methylaminocarbonyl) methoxy] phenyl} -2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 622 [M + H]⁺</li><li>(17) 1- (2- {2 - [(Methoxycarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 639 [M + H]⁺</li><li>(18) 1- (2- {2 - [(Methylaminocarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 638 [M + H]⁺</li><li>(19) 2- (2-acetyl-phenoxy) -N-ethyl-acetamide Mass Spectrum (ESI⁺): m / z = 222 [M + H]⁺</li><li>(20) 1- {2- [2- (1-Methoxycarbonyl-ethoxy) -phenyl] -2-oxo-ethyl} -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 637 [M + H]⁺</li><li>(21) 1- {2- [2- (1-aminocarbonylethoxy) phenyl] -2-oxoethyl} -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 622 [M + H]⁺</li><li>(22) 2- (2-Acetyl-phenoxy) -N-methyl-acetamide Mass Spectrum (ESI⁺): m / z = 208 [M + H]⁺</li><li>(23) 1- {2- [2- (2-Oxo-propoxy) -phenyl] -2-oxo-ethyl} -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 607 [M + H]⁺</li><li>(24) 1- {2- [2- (1-Ethoxycarbonyl-1-methyl-ethoxy) -phenyl] -2-oxo-ethyl} -3-methyl-7- (2-butyn-1-yl) -8 - [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 665 [M + H]⁺</li><li>(25) 1- {2- [2-cyanomethoxyphenyl] -2-oxo-ethyl} -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 590 [M + H]⁺</li><li>(26) 1- (2- {2 - [(Methylsulfanyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8- [3- ( tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 611 [M + H]⁺</li><li>(27) 1 - {[2- (tert-Butylcarbonyl) -benzofuran-3-yl] methyl} -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert. butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Formed as the major product in the reaction of 1- [2- (2-hydroxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- ( tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine with 1-chloro-3,3-dimethyl-butan-2-one) Mass Spectrum (ESI⁺): m / z = 631 [M + H]⁺</li></ol>

Example III

1- [2- (2-hydroxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino ) piperidin-1-yl] -xanthine

0033To a mixture of 2.51 g of 1- [2- (2-hydroxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8-chloro xanthine and 880 mg of sodium carbonate in 8 ml of dimethyl sulfoxide are added 1.30 g of 3-tert-butyloxycarbonylamino-piperidine. The reaction mixture is stirred at 60 ° C for 18 hours. For workup, it is mixed with water and the precipitate is filtered off with suction. The solid crude product is dissolved in ethyl acetate, the solution dried over magnesium sulfate and concentrated. The flask residue is chromatographed on a silica gel column with cyclohexane / ethyl acetate (10: 1 to 1: 1) as the eluent. Yield: 2.56 g (91% of theory) Mass Spectrum (ESI⁺): m / z = 567 [M + H]⁺

0034The following compounds are obtained analogously to Example III:<ol id="ol0005"><li>(1) 3-Methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 433 [M + H]⁺</li><li>(2) 1- (1-Methyl-2-oxo-2-phenylethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert. butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 565 [M + H]⁺</li><li>(3) 3-Methyl-7- (2-cyano-benzyl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.90 (silica gel, methylene chloride / methanol = 9: 1) Mass Spectrum (ESI^-): m / z = 478 [MH]^-</li><li>(4) 1-Methyl-3 - [(methoxycarbonyl) methyl] -7- (2-cyano-benzyl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 552 [M + H]⁺</li><li>(5) 1-Methyl-3-cyanomethyl-7- (2-cyano-benzyl) -8- [3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 519 [M + H]⁺</li><li>(6) 1-Methyl-3- (2-propyn-1-yl) -7- (2-cyano-benzyl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 518 [M + H]⁺</li><li>(7) 1- [2- (3-nitro-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert .-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.25 (silica gel, cyclohexane / ethyl acetate / methanol = 7: 2: 1) Mass Spectrum (ESI⁺): m / z = 596 [M + H]⁺</li><li>(8) 1-Methyl-3- (2-propen-1-yl) -7- (2-cyano-benzyl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 520 [M + H]⁺</li><li>(9) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl ] xanthine Mass Spectrum (ESI⁺): m / z = 535 [M + H]⁺</li><li>(10) 1- [2- (2-nitrophenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert .-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.52 (silica gel, cyclohexane / ethyl acetate = 3: 7) Mass Spectrum (ESI⁺): m / z = 596 [M + H]⁺</li><li>(11) 1-Methyl-3-phenyl-7- (2-cyano-benzyl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 556 [M + H]⁺</li><li>(12) 1- [2- (2-nitro-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 596 [M + H]⁺</li><li>(13) 1 - [(Cinnolin-4-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidine 1-yl] -xanthine in admixture with 1 - [(1,4-dihydro-cinnolin-4-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.62 (silica gel, ethyl acetate)</li><li>(14) 1 - ({4-Oxo-3 - [(2-trimethylsilanylethoxy) methyl] -3,4-dihydro-phthalazin-1-yl} -methyl) -3-methyl-7- (3-methyl -2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Carrying out with potassium carbonate in the presence of Hünigbase) R_fValue: 0.27 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 720 [M + H]⁺</li><li>(15) 1 - [(isoquinolin-3-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.31 (silica gel, ethyl acetate / petroleum ether = 7: 3) Mass Spectrum (ESI⁺): m / z = 574 [M + H]⁺</li><li>(16) 1 - [(3-Methyl-4-oxo-3,4-dihydro-phthalazin-1-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) - 8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.45 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 95: 5) Mass Spectrum (ESI⁺): m / z = 605 [M + H]⁺</li><li>(17) 3-Methyl-7- (2,3-dimethyl-2-buten-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Carrying out with potassium carbonate) R_fValue: 0.42 (silica gel, methylene chloride / methanol = 20: 1) Mass Spectrum (ESI⁺): m / z = 447 [M + H]⁺</li><li>(18) 3-Methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Carrying out with potassium carbonate) Melting point: 235-237 ° C Mass Spectrum (ESI⁺): m / z = 417 [M + H]⁺</li><li>(19) 1 - [(quinolin-4-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] xanthine (Carrying out with potassium carbonate) R_fValue: 0.36 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 558 [M + H]⁺</li><li>(20) 1 - [(isoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] xanthine (Carrying out with potassium carbonate) R_fValue: 0.71 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 558 [M + H]⁺</li><li>(21) 1 - [(isoquinolin-1-yl) methyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidine 1-yl] -xanthine (Carrying out with potassium carbonate, the product contains about 20% Z-isomer) R_fValue: 0.24 (silica gel, ethyl acetate / petroleum ether = 1: 1) Mass Spectrum (ESI⁺): m / z = 560 [M + H]⁺</li><li>(22) 3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Carrying out with potassium carbonate) R_fValue: 0.64 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 417 [M + H]⁺</li><li>(23) 3-methyl-7- (2-butyn-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Carrying out with potassium carbonate) R_fValue: 0.64 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 417 [M + H]⁺</li><li>(24) 3-methyl-7 - ((E) -2-buten-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Product contains about 15% Z-isomer) R_fValue: 0.35 (silica gel, cyclohexane / ethyl acetate = 3: 7) Mass Spectrum (ESI⁺): m / z = 419 [M + H]⁺</li><li>(25) 3-methyl-7 - ((E) -2-buten-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Product contains about 15% Z-isomer) R_fValue: 0.35 (silica gel, cyclohexane / ethyl acetate = 3: 7) Mass Spectrum (ESI⁺): m / z = 419 [M + H]⁺</li><li>(26) 1- [2- (2-Hydroxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 551 [M + H]⁺</li><li>(27) 1- [2- (2-Amino-phenyl) -2-oxo-ethyl] -3-methyl-7 - [(1-cyclopenten-1-yl) -methyl] -8- [3- (tert. -Butyloxycarbonylamino) piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 578 [M + H]⁺</li><li>(28) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7 - [(1-cyclopenten-1-yl) methyl] -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 563 [M + H]⁺</li><li>(29) 1- [2- (2-Hydroxy-phenyl) -2-oxo-ethyl] -3-methyl-7 - [(1-cyclopenten-1-yl) methyl] -8- [3- (tert. -Butyloxycarbonylamino) piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 579 [M + H]⁺</li><li>(30) 1-Methyl-3-isopropyl-7- (2-cyano-benzyl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 522 [M + H]⁺</li><li>(31) 1- [2- (2-Hydroxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert-butyloxycarbonylamino) piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 551 [M + H]⁺</li><li>(32) 1- [2- (2-Amino-phenyl) -2-oxo-ethyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8- [3- (tert .-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Product contains about 10% Z-isomer) R_fValue: 0.20 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 552 [M + H]⁺</li><li>(33) 1- (2-Phenyl-2-oxo-ethyl) -3-methyl-7 - ((E) -2-buten-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine -1-yl] -xanthine (Product contains about 25% Z-isomer) Mass Spectrum (ESI⁺): m / z = 537 [M + H]⁺</li><li>(34) 1- [2- (2-Hydroxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine</li><li>(35) 1- [2- (2-Hydroxy-phenyl) -2-oxo-ethyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8- [3- (tert .-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Product contains some Z-isomer) R_fValue: 0.30 (silica gel, cyclohexane / ethyl acetate = 4: 6) Mass Spectrum (ESI⁺): m / z = 553 [M + H]⁺</li><li>(36) 1- [2- (2-Hydroxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 551 [M + H]⁺</li><li>(37) 1- [2- (2-Amino-phenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) piperidin-1-yl] -xanthine R_fValue: 0.50 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 550 [M + H]⁺</li><li>(38) 1- [2- (2-Hydroxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 567 [M + H]⁺</li><li>(39) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 535 [M + H]⁺</li><li>(40) 1-Methyl-3 - [(2-trimethylsilanylethoxy) methyl] -7- (2-cyano-benzyl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 610 [M + H]⁺</li><li>(41) 3-methyl-7- (2-butyn-1-yl) -8 - [(<i>S</i>) - 3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Carrying out with potassium carbonate) R_fValue: 0.52 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 417 [M + H]⁺</li><li>(42) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7- (2-methyl-allyl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] - xanthine R_fValue: 0.46 (silica gel, methylene chloride / methanol = 95: 5)</li><li>(43) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7- (3-bromo-allyl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] - xanthine R_fValue: 0.22 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 601, 603 [M + H]⁺</li><li>(44) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7 - [(furan-2-yl) methyl] -8- [3- (tert -butyloxycarbonylamino) -piperidine-1. yl] -xanthine R_f-Wert: 0.41 (Kieselgel, Methylenchlorid/Methanol = 95:5)</li><li>(45) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7- (2-chloro-allyl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] - xanthine R_fValue: 0.49 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 557, 559 [M + H]⁺</li><li>(46) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 535 [M + H]⁺</li><li>(47) 1- [2- (2-Amino-phenyl) -2-oxo-ethyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.40 (silica gel, cyclohexane / ethyl acetate = 4: 6) Mass Spectrum (ESI⁺): m / z = 552 [M + H]⁺</li><li>(48) 1- [2- (2-nitro-phenyl) -2-oxo-ethyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.50 (silica gel, cyclohexane / ethyl acetate = 1: 2)</li><li>(49) 1- [2- (2-nitro-phenyl) -2-oxo-ethyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 582 [M + H]⁺</li><li>(50) 1- [2- (2-nitro-3-methoxyphenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- 3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 626 [M + H]⁺</li><li>(51) 1- (2- {2-Oxo-3 - [(2-trimethylsilanylethoxy) methyl] -2,3-dihydro-benzooxazol-7-yl} -2-oxo-ethyl) -3-methyl- 7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 738 [M + H]⁺</li><li>(52) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7 - ((Z) -2-methyl-2-buten-1-yl) -8- [3- (tert. butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.48 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 551 [M + H]⁺</li><li>(53) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7 - ((E) -2-methyl-2-buten-1-yl) -8- [3- (tert. butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 551 [M + H]⁺</li><li>(54) 1- (2- {2-Oxo-3 - [(2-trimethylsilanylethoxy) methyl] -2,3-dihydro-benzooxazol-4-yl} -2-oxo-ethyl) -3-methyl- 7- (2-butyn-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.40 (silica gel, petroleum ether / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 722 [M + H]⁺</li><li>(55) 1- [2- (2,2-Difluoro-benzo [1,3] dioxol-4-yl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8th-[(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 615 [M + H]⁺</li><li>(56) 1- [2- (2,2-Difluoro-benzo [1,3] dioxol-4-yl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8th-[(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 615 [M + H]⁺</li><li>(57) 1 - [(1-methyl-1<i>H</i>indol-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.80 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 560 [M + H]⁺</li><li>(58) 1 - [(quinolin-3-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] xanthine R_fValue: 0.50 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 558 [M + H]⁺</li><li>(59) 1 - {[1- (tert-Butyloxycarbonylamino) -1<i>H</i>indol-2-yl] methyl} -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.40 (silica gel, petroleum ether / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 646 [M + H]⁺</li><li>(60) 1 - [(2-Methyl-1 - [(2-trimethylsilanylethoxy) methyl] -1<i>H</i>benzoimidazol-5-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine (in admixture with 1 - [(2-methyl-3 - [(2-trimethylsilanyl-ethoxy) methyl] -3<i>H</i>-benzoimidazol-5-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine) R_fValue: 0.15 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 691 [M + H]⁺</li><li>(61) 1- [2- (quinolin-8-yl] - 2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino ) piperidin-1-yl] -xanthine R_fValue: 0.35 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 586 [M + H]⁺</li><li>(62) 1 - [(1 - [(2-trimethylsilanylethoxy) methyl] -1<i>H</i>benzoimidazol-5-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine (in admixture with 1 - [(3 - [(2-trimethylsilanyl-ethoxy) methyl] -3<i>H</i>-benzoimidazol-5-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine) R_fValue: 0.23 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 677 [M + H]⁺</li><li>(63) 1 - [(pyrazolo [1,5-a] pyridin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino ) piperidin-1-yl] -xanthine R_fValue: 0.46 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 547 [M + H]⁺</li><li>(64) 1- (2-Phenyl-2-oxo-ethyl) -3-methyl-7 - ((E) -1-buten-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine -1-yl] -xanthine R_fValue: 0.48 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 537 [M + H]⁺</li><li>(65) 1- {2- [1- (tert -butyloxycarbonyl) -1<i>H</i>-indol-7-yl] -2-oxo-ethyl} -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] - xanthine R_fValue: 0.38 (silica gel, petroleum ether / ethyl acetate = 1: 1)</li><li>(66) 1 - [(3-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (3-methyl-1-buten-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.40 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 588 [M + H]⁺</li><li>(67) 1,3-Dimethyl-7- (2-bromo-benzyl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.40 (silica gel, cyclohexane / ethyl acetate = 1: 1)</li><li>(68) 1,3-Dimethyl-7- (2-chloro-benzyl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.42 (silica gel, cyclohexane / ethyl acetate = 1: 1)</li><li>(69) 1 - [(3-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-cyano-benzyl) -8- [3- (tert -butyloxycarbonylamino) -piperidine-1. yl] -xanthine Mass Spectrum (ESI⁺): m / z = 635 [M + H]⁺R_fValue: 0.40 (silica gel, cyclohexane / ethyl acetate = 3: 7)</li><li>(70) 3-Cyclopropyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 443 [M + H]⁺R_fValue: 0.70 (silica gel, ethyl acetate)</li><li>(71) 3-Cyclopropyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.35 (reversed phase DC precast plate (E. Merck), acetonitrile / water / trifluoroacetic acid = 50: 50: 1) Mass Spectrum (ESI⁺): m / z = 443 [M + H]⁺</li><li>(72) 1 - [(3-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-chloro-benzyl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 644, 646 [M + H]⁺R_fValue: 0.39 (silica gel, cyclohexane / ethyl acetate = 1: 1)</li><li>(73) 1 - [(3-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-bromo-benzyl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 644, 646 [M + H]⁺</li><li>(74) 1 - [(4-Methyl-quinazolin-2-yl) methyl] -3-methyl-7- (2-chloro-benzyl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Prepared by reaction of (4-methyl-quinazolin-2-yl) -methyl chloride and 3-methyl-7- (2-chloro-benzyl) -8-bromo-xanthine and subsequent reaction with (<i>R</i>) -3- (tert-butyloxycarbonylamino) piperidine Mass Spectrum (ESI⁺): m / z = 645, 647 [M + H]⁺</li><li>(75) 1 - [(4-phenyl-quinazolin-2-yl) methyl] -3-methyl-7- (2-chloro-benzyl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Prepared by reaction of (4-phenyl-quinazolin-2-yl) -methyl chloride and 3-methyl-7- (2-chloro-benzyl) -8-bromo-xanthine and subsequent reaction with (<i>R</i>) -3- (tert-butyloxycarbonylamino) piperidine Mass Spectrum (ESI⁺): m / z = 707, 709 [M + H]⁺</li></ol>

Example IV

1- [2- (2-hydroxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8-chloro-xanthine

0035prepared by treating 1- [2- (2-methoxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8-chloro-xanthine with Boron tribromide in methylene chloride. The desired product is with about 20% of 1- [2- (2-hydroxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-bromo-3-methylbutyl) -8-chloro xanthine contaminated. Mass Spectrum (ESI⁺): m / z = 403, 405 [M + H]⁺

0036Analogously to Example IV, the following compounds are obtained:<ol id="ol0006"><li>(1) 1- [2- (2-Hydroxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8-bromo-xanthine (product is with approx. 20% of 1- [2- (2-hydroxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-bromo-2-buten-1-yl) -8-bromo-xanthine contaminated) Mass Spectrum (ESI⁺): m / z = 431, 433 [M + H]⁺</li><li>(2) 1- [2- (2-Hydroxy-phenyl) -2-oxo-ethyl] -3-methyl-7 - [(1-cyclopenten-1-yl) methyl] -8-bromo-xanthine Mass Spectrum (ESI⁺): m / z = 459, 461 [M + H]⁺</li><li>(3) 1- [2- (2-Hydroxy-phenyl) -2-oxo-ethyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8-bromo-xanthine (Product contains some Z-isomer) R_fValue: 0.60 (silica gel, cyclohexane / ethyl acetate = 4: 6) Mass Spectrum (ESI⁺): m / z = 433, 435 [M + H]⁺</li><li>(4) 1- [2- (2-Hydroxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8-bromxanthine Mass Spectrum (ESI⁺): m / z = 447, 449 [M + H]⁺</li></ol>

Example V

1- [2- (2-methoxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8-chloro-xanthine

0037To a mixture of 2.00 g of 3-methyl-7- (3-methyl-2-buten-1-yl) -8-chloro-xanthine and 1.38 mg of potassium carbonate in 15 ml of N, N-dimethylformamide are added 1.71 g of 2-bromo- Added 1- (2-methoxy-phenyl) -ethanone. The reaction mixture is stirred for eight hours at room temperature. After aqueous workup, the crude product is purified by chromatography on a silica gel column with cyclohexane / ethyl acetate (8: 1 to 8: 1) as the eluent. Yield: 2.61 g (84% of theory) Mass Spectrum (ESI⁺): m / z = 417, 419 [M + H]⁺

0038Analogously to Example V, the following compounds are obtained:<ul id="ul0002" list-style="none"><li>(1) 1- [2- (3-Hydroxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert .-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (The reaction is carried out with 2-bromo-1- [3- (tert-butyldimethylsilanyloxy) -phenyl] -ethanone) R_fValue: 0.40 (silica gel, cyclohexane / ethyl acetate = 3: 7) Mass Spectrum (ESI⁺): m / z = 567 [M + H]⁺</li><li>(2) 1- (1-Methyl-2-oxo-2-phenylethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8-chlorxanthine Mass Spectrum (ESI⁺): m / z = 401, 403 [M + H]⁺</li><li>(3) 1- (2-Cyanoethyl) -3-methyl-7- (2-cyanobenzyl) -8-chloro-xanthine Mass Spectrum (ESI⁺): m / z = 391, 393 [M + Na]⁺</li><li>(4) 1- (2-Phenoxyethyl) -3-methyl-7- (2-cyano-benzyl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.90 (silica gel, methylene chloride / methanol = 9: 1) Mass Spectrum (ESI⁺): m / z = 600 [M + H]⁺</li><li>(5) 1- (2-phenyl-2-oxo-ethyl) -3 - [(2-trimethylsilanylethoxy) methyl] -7- (3-methyl-2-buten-1-yl) -8- [3 - (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 667 [M + H]⁺</li><li>(6) 1- (2-Methoxyethyl) -3-methyl-7- (2-cyano-benzyl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.90 (silica gel, methylene chloride / methanol = 9: 1) Mass Spectrum (ESI⁺): m / z = 538 [M + H]⁺</li><li>(7) 1-Methyl-3 - [(2-trimethylsilanylethoxy) methyl] -7- (2-cyano-benzyl) -xanthine R_fValue: 0.60 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 412 [M + H]⁺</li><li>(8) 1- [2- (3-nitrophenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8-chlorxanthine R_fValue: 0.40 (silica gel, cyclohexane / ethyl acetate / methanol = 7: 2: 1) Mass Spectrum (ESI⁺): m / z = 432, 434 [M + H]⁺</li><li>(9) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7 - [(2-trimethylsilanylethoxy) methyl] -8-bromxanthine Mass Spectrum (ESI⁺): m / z = 493, 495 [M + H]⁺</li><li>(10) 1- [2- (2-nitrophenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8-chlorxanthine R_fValue: 0.64 (silica gel, cyclohexane / ethyl acetate = 3: 7) Mass Spectrum (ESI⁺): m / z = 432, 434 [M + H]⁺</li><li>(11) 1- [2- (2-nitrophenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8-bromxanthine Mass Spectrum (ESI⁺): m / z = 476, 478 [M + H]⁺</li><li>(12) 1 - [(quinolin-2-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.45 (silica gel, ethyl acetate / petroleum ether = 7: 3) Mass Spectrum (ESI⁺): m / z = 574 [M + H]⁺</li><li>(13) 1 - [(2-oxo-2<i>H</i>chromen-4-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (The starting material 4-bromomethyl-chromen-2-one is analogous <nplcit id="ncit0003" npl-type="s"><text>Kimura et al., Chem. Pharm. Bull. 1982, 30, 552-558</text></nplcit> manufactured.) R_fValue: 0.52 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 591 [M + H]⁺</li><li>(14) 1 - [(1-Methyl-2-oxo-1,2-dihydroquinolin-4-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) - 8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.54 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 604 [M + H]⁺</li><li>(15) 1 - [(Quinazolin-4-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine Melting point: 195-197 ° C Mass Spectrum (ESI⁺): m / z = 575 [M + H]⁺</li><li>(16) 1 - [(5-Methyl-3-phenyl-isoxazol-4-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- ( tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.40 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 604 [M + H]⁺</li><li>(17) 1 - [(3-Phenyl- [1,2,4] oxadiazol-5-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [ 3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.18 (silica gel, petroleum ether / ethyl acetate = 2: 1) Mass Spectrum (ESI⁺): m / z = 591 [M + H]⁺</li><li>(18) 1 - [(4-phenylpyridin-2-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert-butyloxycarbonylamino ) piperidin-1-yl] -xanthine R_fValue: 0.53 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 600 [M + H]⁺</li><li>(19) 1 - [(5-phenylpyridin-2-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert-butyloxycarbonylamino ) piperidin-1-yl] -xanthine R_fValue: 0.73 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 600 [M + H]⁺</li><li>(20) 1- [2- (3-Methylsulfanyl-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert .-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.43 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 597 [M + H]⁺</li><li>(21) 1- [2- (3-Methoxycarbonyl-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert .-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Procedure in N-methylpyrrolidin-2-one at 60 ° C) R_fValue: 0.27 (silica gel, methylene chloride / methanol = 20: 1) Mass Spectrum (ESI⁺): m / z = 609 [M + H]⁺</li><li>(22) 1- [2- (2-ethoxycarbonyl-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert .-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Procedure in N-methylpyrrolidin-2-one at 60 ° C) R_fValue: 0.35 (silica gel, methylene chloride / methanol = 20: 1) Mass Spectrum (ESI⁺): m / z = 623 [M + H]⁺</li><li>(23) 1- [2- (2,6-dimethoxyphenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3 (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Procedure in N-methylpyrrolidin-2-one at 60 ° C) R_fValue: 0.53 (silica gel, methylene chloride / methanol = 20: 1) Mass Spectrum (ESI⁺): m / z = 611 [M + H]⁺</li><li>(24) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7- (2,3-dimethyl-2-buten-1-yl) -8- [3- (tert-butyloxycarbonylamino) piperidin-1-yl] -xanthine (Procedure in N-methylpyrrolidin-2-one at 60 ° C) R_fValue: 0.38 (silica gel, methylene chloride / methanol = 20: 1) Mass Spectrum (ESI⁺): m / z = 565 [M + H]⁺</li><li>(25) 1 - ((E) -3-phenyl-allyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine -1-yl] -xanthine R_fValue: 0.54 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 95: 5: 0.1) Mass Spectrum (ESI⁺): m / z = 549 [M + H]⁺</li><li>(26) 1 - [(1-benzo [<i>b</i>] Thiophen-3-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.75 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 579 [M + H]⁺</li><li>(27) 1 - {[1- (tert-Butyloxycarbonyl) indol-3-yl] methyl} -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.61 (silica gel, methylene chloride / methanol = 9: 1) Mass Spectrum (ESI⁺): m / z = 662 [M + H]⁺</li><li>(28) 1 - [(Biphenyl-4-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.68 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 599 [M + H]⁺</li><li>(29) 1 - [(1-Naphthyl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.83 (silica gel, ethyl acetate / petroleum ether = 4: 1) Mass Spectrum (ESI⁺): m / z = 557 [M + H]⁺</li><li>(30) 1 - [(1-Methyl-2-oxo-1,2-dihydroquinolin-4-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3 - (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.25 (silica gel, ethyl acetate / petroleum ether = 4: 1) Mass Spectrum (ESI⁺): m / z = 588 [M + H]⁺</li><li>(31) 1- (2-Cyclohexyl-2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine -1-yl] -xanthine Melting point: 163-165 ° C Mass Spectrum (ESI⁺): m / z = 557 [M + H]⁺</li><li>(32) 1- (3,3-Dimethyl-2-oxobutyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert-butyloxycarbonylamino) piperidin-1-yl] -xanthine R_fValue: 0.95 (silica gel, ethyl acetate / petroleum ether = 4: 1) Mass Spectrum (ESI⁺): m / z = 531 [M + H]⁺</li><li>(33) 1 - [(quinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] xanthine R_fValue: 0.40 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 559 [M + H]⁺</li><li>(34) 1 - [(2-Methyl-naphthalen-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.80 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 571 [M + H]⁺</li><li>(35) 1 - [(5-nitro-isoquinolin-1-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert -butyloxycarbonylamino ) piperidin-1-yl] -xanthine R_fValue: 0.54 (silica gel, methylene chloride / methanol = 95: 5)</li><li>(36) 1- (2-Dimethylamino-2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine -1-yl] -xanthine R_fValue: 0.23 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 518 [M + H]⁺</li><li>(37) 1- [2- (piperidin-1-yl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert .-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.44 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 558 [M + H]⁺</li><li>(38) 1 - [(2-Methyl-1-oxo-1,2-dihydroisoquinolin-4-yl) methyl] -7- (2-butyn-1-yl) -8- [3- (tert. -Butyloxycarbonylamino) piperidin-1-yl] -xanthine R_fValue: 0.25 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 588 [M + H]⁺</li><li>(39) 1 - [(2-Methyl-1-oxo-1,2-dihydro-isoquinolin-4-yl) methyl] -7- (3-methyl-2-buten-1-yl) -8- [3 - (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.30 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 604 [M + H]⁺</li><li>(40) 1 - [(2-methoxynaphthalene-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.75 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 587 [M + H]⁺</li><li>(41) 1 - [(4-methoxynaphthalene-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.80 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 587 [M + H]⁺</li><li>(42) 1 - [(3-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.56 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 572 [M + H]⁺</li><li>(43) 1- [2- (2,3-Dimethoxyphenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.83 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 611 [M + H]⁺</li><li>(44) 1 - [(5-nitro-naphthalen-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.78 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 602 [M + H]⁺</li><li>(45) 1- [2- (pyrrolidin-1-yl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert .-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.39 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 544 [M + H]⁺</li><li>(46) 1 - [(4-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.56 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 572 [M + H]⁺</li><li>(47) 1 - [(2-Naphthyl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.78 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 557 [M + H]⁺</li><li>(48) 1-Cyanomethyl-3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.80 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 456 [M + H]⁺</li><li>(49) 1 - [(quinolin-6-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] xanthine R_fValue: 0.40 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 558 [M + H]⁺</li><li>(50) 1 - [(3-methoxynaphthalene-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.83 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 587 [M + H]⁺</li><li>(51) 1- [2- (2,3-dihydro-benzo [1,4] dioxin-5-yl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-butene 1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.38 (silica gel, ethyl acetate / petroleum ether = 1: 1) Mass Spectrum (ESI⁺): m / z = 609 [M + H]⁺</li><li>(52) 1- [2- (3-methyl-2-oxo-2,3-dihydro-benzooxazol-7-yl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-) buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Carrying out with potassium tert-butoxide in dimethyl sulfoxide) R_fValue: 0.48 (silica gel, ethyl acetate / petroleum ether = 2: 1) Mass Spectrum (ESI⁺): m / z = 622 [M + H]⁺</li><li>(53) 1- [2- (Benzo [1,3] dioxol-4-yl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8 - [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 595 [M + H]⁺</li><li>(54) 1 - [(quinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 559 [M + H]⁺</li><li>(55) 1 - [(quinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 559 [M + H]⁺</li><li>(56) 1 - [(quinazolin-2-yl) methyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Product contains about 15% Z-isomer) R_fValue: 0.30 (silica gel, ethyl acetate / cyclohexane = 8: 2) Mass Spectrum (ESI⁺): m / z = 561 [M + H]⁺</li><li>(57) 1 - [(quinazolin-2-yl) methyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Product contains about 15% Z-isomer) R_fValue: 0.30 (silica gel, ethyl acetate / cyclohexane = 8: 2) Mass Spectrum (ESI⁺): m / z = 561 [M + H]⁺</li><li>(58) 1 - [(3-methylisoquinolin-1-yl) methyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Product contains about 17% Z-isomer) R_fValue: 0.58 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 574 [M + H]⁺</li><li>(59) 1 - [(3-methylisoquinolin-1-yl) methyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Product contains about 17% Z-isomer) R_fValue: 0.58 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 574 [M + H]⁺</li><li>(60) 1- [2- (2-Methoxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8-bromo-xanthine Mass Spectrum (ESI⁺): m / z = 445, 447 [M + H]⁺</li><li>(61) 1- [2- (2-nitrophenyl) -2-oxo-ethyl] -3-methyl-7 - [(1-cyclopenten-1-yl) methyl] -8-bromo-xanthine Mass Spectrum (ESI⁺): m / z = 488, 490 [M + H]⁺</li><li>(62) 1- [2- (2-Methoxy-phenyl) -2-oxo-ethyl] -3-methyl-7 - [(1-cyclopenten-1-yl) methyl] -8-bromo-xanthine Mass Spectrum (ESI⁺): m / z = 473, 475 [M + H]⁺</li><li>(63) 1 - [(isoquinolin-1-yl) methyl] -3 - [(methoxycarbonyl) methyl] -7- (3-methyl-2-buten-1-yl) -8- [3- (tert. butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.35 (silica gel, methylene chloride / methanol = 95: 5)</li><li>(64) 1- [2- (2-nitro-phenyl) -2-oxo-ethyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8-bromo-xanthine (Product contains about 10% Z-isomer) R_fValue: 0.60 (silica gel, cyclohexane / ethyl acetate = 4: 6) Mass Spectrum (ESI⁺): m / z = 462, 464 [M + H]⁺</li><li>(65) 1- [2- (2-Methoxy-phenyl) -2-oxo-ethyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8-bromxanthine (Product contains some Z-isomer) R_fValue: 0.30 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 447, 449 [M + H]⁺</li><li>(66) 1- [2- (2-nitrophenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8-bromo-xanthine R_fValue: 0.77 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 460, 462 [M + H]⁺</li><li>(67) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7 - ((E) -2-buten-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Product contains about 20% Z-isomer) Mass Spectrum (ESI⁺): m / z = 537 [M + H]⁺</li><li>(68) 1- [2- (2-Methoxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8-bromxanthine Mass Spectrum (ESI⁺): m / z = 461, 463 [M + H]⁺</li><li>(69) 1- (2-Phenyl-2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8-bromo-xanthine R_fValue: 0.61 (silica gel, cyclohexane / ethyl acetate = 4: 6)</li><li>(70) 1- (2- {2 - [(ethylaminocarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7 - ((E) -2-buten-1-yl) -8- [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Product contains about 17% Z-isomer) Mass Spectrum (ESI⁺): m / z = 638 [M + H]⁺</li><li>(71) 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7 - ((E) -2-buten-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Product contains about 18% Z-isomer) R_fValue: 0.35 (silica gel, cyclohexane / ethyl acetate = 6: 4) Mass Spectrum (ESI⁺): m / z = 537 [M + H]⁺</li><li>(72) 1- [2- (2-nitrophenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.60 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 580 [M + H]⁺</li><li>(73) 1 - [(3-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.52 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 572 [M + H]⁺</li><li>(74) 1 - [(3-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 572 [M + H]⁺</li><li>(75) 1 - [(4-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 572 [M + H]⁺</li><li>(76) 1 - [(4-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 572 [M + H]⁺</li><li>(77) 1 - [(4-Methylisoquinolin-1-yl) methyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.52 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 574 [M + H]⁺</li><li>(78) 1 - [(4-Methylisoquinolin-1-yl) methyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.52 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 574 [M + H]⁺</li><li>(79) 1- [2- (2,3-dihydro-benzo [1,4] dioxin-5-yl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8th-[(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.18 (silica gel, ethyl acetate / petroleum ether = 1: 1) Mass Spectrum (ESI⁺): m / z = 593 [M + H]⁺</li><li>(80) 1- [2- (2,3-dihydro-benzo [1,4] dioxin-5-yl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8th-[(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 593 [M + H]⁺</li><li>(81) 1 - [(4-methoxynaphthalen-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.56 (silica gel, petroleum ether / ethyl acetate = 1: 2) Mass Spectrum (ESI⁺): m / z = 587 [M + H]⁺</li><li>(82) 1 - [(4-methoxynaphthalen-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 587 [M + H]⁺</li><li>(83) 1- [2- (benzo [1,3] dioxol-4-yl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.86 (silica gel, ethyl acetate / petroleum ether = 4: 1) Mass Spectrum (ESI⁺): m / z = 579 [M + H]⁺</li><li>(84) 1- [2- (benzo [1,3] dioxol-4-yl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.86 (silica gel, ethyl acetate / petroleum ether = 4: 1) Mass Spectrum (ESI⁺): m / z = 579 [M + H]⁺</li><li>(85) 1 - [(4-methylquinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.48 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 573 [M + H]⁺</li><li>(86) 1 - [(4-methylquinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.48 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 573 [M + H]⁺</li><li>(87) 1- [2- (3-Methyl-2-oxo-2,3-dihydro-benzooxazol-4-yl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-) buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.50 (silica gel, petroleum ether / ethyl acetate = 1: 2) Mass Spectrum (ESI⁺): m / z = 622 [M + H]⁺</li><li>(88) 1- (2- {2 - [(ethylaminocarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7 - ((E) -2-buten-1-yl) -8- [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 638 [M + H]⁺</li><li>(89) 1- (2- {2 - [(Methylaminocarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7 - ((E) -2-buten-1-yl) -8- [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 624 [M + H]⁺</li><li>(90) 1- (2- {2 - [(Methylaminocarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7 - ((E) -2-buten-1-yl) -8- [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 624 [M + H]⁺</li><li>(91) 1- [2- (2-nitrophenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.60 (silica gel, methylene chloride / methanol = 95: 5)</li><li>(92) 1- [2- (2-nitro-3-methoxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8-bromo xanthine Mass Spectrum (ESI⁺): m / z = 506, 508 [M + H]⁺</li><li>(93) 1 - [(4-Dimethylamino-quinolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine (Carrying out in the presence of cesium carbonate) R_fValue: 0.40 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 602 [M + H]⁺</li><li>(94) 1- (2- {2-Oxo-3 - [(2-trimethylsilanylethoxy) methyl] -2,3-dihydro-benzooxazol-7-yl} -2-oxo-ethyl) -3-methyl- 7- (3-methyl-2-buten-1-yl) -8-bromo-xanthine R_fValue: 0.75 (silica gel, ethyl acetate / petroleum ether = 1: 1) Mass Spectrum (ESI⁺): m / z = 618, 620 [M + H]⁺</li><li>(95) 1 - [(Imidazo [1,2-a] pyridin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino ) piperidin-1-yl] -xanthine R_fValue: 0.44 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 547 [M + H]⁺</li><li>(96) 1 - [(quinoxalin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] xanthine R_fValue: 0.50 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 559 [M + H]⁺</li><li>(97) 1- [2- (1,3-dimethyl-2-oxo-2,3-dihydro-1H-benzoimidazol-4-yl) -2-oxo-ethyl] -3-methyl-7- (2- butyn-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.50 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 619 [M + H]⁺</li><li>(98) 1 - [(quinoxalin-6-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] xanthine R_fValue: 0.35 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 559 [M + H]⁺</li><li>(99) 1- (2- {2-Oxo-3 - [(2-trimethylsilanylethoxy) methyl] -2,3-dihydro-benzooxazol-4-yl} -2-oxo-ethyl) -3-methyl- 7- (2-butyn-1-yl) -8-bromo-xanthine R_fValue: 0.30 (silica gel, petroleum ether / ethyl acetate = 2: 1) Mass Spectrum (ESI^-): m / z = 600, 602 [MH]^-</li><li>(100) 1 - [(3-Methyl-quinoxalin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.44 (silica gel, petroleum ether / ethyl acetate = 1: 2) Mass Spectrum (ESI⁺): m / z = 573 [M + H]⁺</li><li>(101) 1 - [(3-Phenylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.85 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 634 [M + H]⁺</li><li>(102) 1 - [(3,4-Dimethylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) - piperidin-1-yl] -xanthine R_fValue: 0.60 (silica gel, ethyl acetate / methanol = 3: 1) Mass Spectrum (ESI⁺): m / z = 586 [M + H]⁺</li><li>(103) 1 - [(Benzofuran-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 547 [M + H]⁺</li><li>(104) 1 - {[4- (morpholin-4-yl) -quinazolin-2-yl] methyl} -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert. -Butyloxycarbonylamino) piperidin-1-yl] -xanthine (Carrying out in the presence of cesium carbonate) R_fValue: 0.28 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 644 [M + H]⁺</li><li>(105) 1 - {[4- (piperidin-1-yl) quinazolin-2-yl] methyl} -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert. -Butyloxycarbonylamino) piperidin-1-yl] -xanthine (Carrying out in the presence of cesium carbonate) R_fValue: 0.35 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 642 [M + H]⁺</li><li>(106) 1 - ({4- [4- (tert-Butyloxycarbonyl) piperazin-1-yl] quinazolin-2-yl} methyl) -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Carrying out in the presence of cesium carbonate) R_fValue: 0.50 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 743 [M + H]⁺</li><li>(107) 1 - {[4- (Pyrrolidin-1-yl) -quinazolin-2-yl] methyl} -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert. -Butyloxycarbonylamino) piperidin-1-yl] -xanthine (Carrying out in the presence of cesium carbonate) R_fValue: 0.59 (silica gel, ethyl acetate / methanol / concentrated aqueous ammonia = 95: 5: 0.1) Mass Spectrum (ESI⁺): m / z = 628 [M + H]⁺</li><li>(108) 1- [2- (1-Ethoxycarbonyl-3-methyl-2-oxo-2,3-dihydro-1H-benzoimidazol-4-yl) -2-oxo-ethyl] -3-methyl-7- ( 2-butyn-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.25 (silica gel, petroleum ether / ethyl acetate = 1: 2) Mass Spectrum (ESI⁺): m / z = 677 [M + H]⁺</li><li>(109) 1 - [(4-cyano-naphthalen-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.77 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 582 [M + H]⁺</li><li>(110) 1 - [(imidazo [1,2-a] pyridin-3-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert-butyloxycarbonylamino ) piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 547 [M + H]⁺</li><li>(111) 1 - [(8-Methylimidazo [1,2-a] pyridin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- ( tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.25 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 561 [M + H]⁺</li><li>(112) 1 - [(8-Methoxyquinolin-5-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine. 1-yl] -xanthine R_fValue: 0.60 (silica gel, ethyl acetate / methanol = 9: 1) Mass Spectrum (ESI⁺): m / z = 588 [M + H]⁺</li><li>(113) 1 - [(5-Methoxyquinolin-8-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.40 (silica gel, methylene chloride / methanol = 20: 1) Mass Spectrum (ESI⁺): m / z = 588 [M + H]⁺</li><li>(114) 1 - [(4-phenyl-quinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine. 1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 635 [M + H]⁺</li><li>(115) 1 - [(7-Methylimidazo [1,2-a] pyridin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- ( tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.50 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 561 [M + H]⁺</li><li>(116) 1- (2-Oxo-4-phenylbutyl) -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 563 [M + H]⁺</li><li>(117) 1- (2- {2-Oxo-1,3-bis - [(2-trimethylsilanylethoxy) methyl] -2,3-dihydro-1<i>H-</i>benzoimidazol-4-yl} -2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.50 (silica gel, ethyl acetate / petroleum ether = 1: 1) Mass Spectrum (ESI⁺): m / z = 851 [M + H]⁺</li><li>(118) 1 - [(3-Difluoromethylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidine 1-yl] -xanthine (By-product in the reaction of 3-methyl-7- (2-butyn-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine with 1-chloromethyl-3-trifluoromethyl -3,4-dihydroisoquinoline) R_fValue: 0.75 (alumina, petroleum ether / ethyl acetate = 1: 2) Mass Spectrum (ESI⁺): m / z = 608 [M + H]⁺</li><li>(119) 1- [2- (2,2-Difluoro-benzo [1,3] dioxol-4-yl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8-bromo-xanthine Mass Spectrum (ESI⁺): m / z = 495, 497 [M + H]⁺</li><li>(120) 1 - [(3-Methylimidazo [1,2-a] pyridin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- ( tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.50 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 561 [M + H]⁺</li><li>(121) 1 - [(5-Methylimidazo [1,2-a] pyridin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- ( tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.50 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 561 [M + H]⁺</li><li>(122) 1 - [(6-Methylimidazo [1,2-a] pyridin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- ( tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.10 (silica gel, ethyl acetate / methanol = 98: 2) Mass Spectrum (ESI⁺): m / z = 561 [M + H]⁺</li><li>(123) 1 - [(3-Benzylimidazo [1,2-a] pyridin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- ( tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.60 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 637 [M + H]⁺</li><li>(124) 1 - [(4-Isopropyl-quinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidine. 1-yl] -xanthine R_fValue: 0.50 (silica gel, ethyl acetate / petroleum ether = 8: 2) Mass Spectrum (ESI⁺): m / z = 601 [M + H]⁺</li><li>(125) 1 - [(2,3-Dihydrobenzo [1,4] dioxin-6-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- ( tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.53 (silica gel, ethyl acetate / petroleum ether = 3: 2)</li><li>(126) 1 - [(3-phenylimidazo [1,2-a] pyridin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- ( tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.50 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 623 [M + H]⁺</li><li>(127) 1- [2- (Naphthalen-1-yl] -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert-butyloxycarbonylamino) piperidin-1-yl] -xanthine R_fValue: 0.54 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 585 [M + H]⁺</li><li>(128) 1 - [(5-Methoxyisoquinolin-8-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.50 (silica gel, ethyl acetate / methanol = 24: 1) Mass Spectrum (ESI⁺): m / z = 588 [M + H]⁺</li><li>(129) 1 - [(3-Difluoromethylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine (By-product in the reaction of 3-methyl-7- (2-butyn-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine with 1-chloromethyl-3-trifluoromethyl -3,4-dihydroisoquinoline) R_fValue: 0.75 (alumina, petroleum ether / ethyl acetate = 1: 2) Mass Spectrum (ESI⁺): m / z = 608 [M + H]⁺</li><li>(130) 1 - {[1- (1-Cyano-1-methylethyl) isoquinolin-3-yl] methyl} -3-methyl-7- (2-butyn-1-yl) -8- [3 - (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.75 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 625 [M + H]⁺</li><li>(132) 1-Methoxycarbonylmethyl-3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 489 [M + H]⁺</li><li>(133) 1 - [(4-phenylquinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 635 [M + H]⁺</li><li>(134) 1 - [(2,3-Dimethyl-quinoxalin-6-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) - piperidin-1-yl] -xanthine (Carrying out in the presence of cesium carbonate) R_fValue: 0.40 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 587 [M + H]⁺</li><li>(135) 1 - [(4-phenylquinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.55 (silica gel, ethyl acetate / petroleum ether = 8: 2) Mass Spectrum (ESI⁺): m / z = 635 [M + H]⁺</li><li>(136) 1- [2- (Quinolin-8-yl] - 2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8-bromo-xanthine R_fValue: 0.55 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 466, 468 [M + H]⁺</li><li>(137) 1 - [(3,4-Dimethyl-6,7-dihydro-5H- [2] pyrindin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.65 (alumina, ethyl acetate / petroleum ether = 3: 1) Mass Spectrum (ESI⁺): m / z = 576 [M + H]⁺</li><li>(138) 1 - [(3,4-dimethyl-5,6,7,8-tetrahydroisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.40 (alumina, methylene chloride / methanol = 20: 1) Mass Spectrum (ESI⁺): m / z = 590 [M + H]⁺</li><li>(139) 1- {2- [1- (tert -butyloxycarbonyl) -1H-indol-4-yl] -2-oxo-ethyl} -3-methyl-7- (2-butyn-1-yl) - 8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.55 (silica gel, petroleum ether / ethyl acetate = 1: 2) Mass Spectrum (ESI⁺): m / z = 674 [M + H]⁺</li><li>(140) 1 - [(1-Methyl-2-oxo-1,2-dihydroquinolin-6-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3 - (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass spectrum (EI): m / z = 587 [M]⁺</li><li>(141) 1 - ({1 - [(2-trimethylsilanylethoxy) methyl] -2-oxo-1,2-dihydro-quinolin-6-yl} methyl) -3-methyl-7- (2-butyne) 1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 704 [M + H]⁺</li><li>(142) 1 - [(2,3,8-trimethyl-quinoxalin-6-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert-butyloxycarbonylamino ) piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 601 [M + H]⁺</li><li>(143) 1 - [(8-Methyl-quinoxalin-6-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 573 [M + H]⁺</li><li>(144) 1 - [(4-Methyl-phthalazin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine. 1-yl] -xanthine R_fValue: 0.65 (silica gel, methylene chloride / methanol = 9: 1) Mass Spectrum (ESI⁺): m / z = 573 [M + H]⁺</li><li>(145) 1 - [(4-Bromo-3-methoxy-isoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino ) piperidin-1-yl] -xanthine R_fValue: 0.65 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 666, 668 [M + H]⁺</li><li>(146) 1 - [(4-Difluoromethoxynaphthalen-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.80 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 623 [M + H]⁺</li><li>(147) 1- {2- [1- (tert-butyloxycarbonyl) -1<i>H</i>-indol-7-yl] -2-oxo-ethyl} -3-methyl-7- (2-butyn-1-yl) -8-bromo-xanthine R_fValue: 0.83 (silica gel, methylene chloride / methanol = 95: 5)</li><li>(148) 1 - [(E) -3- (2-nitrophenyl) -2-propen-1-yl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 578 [M + H]⁺</li><li>(149) 1 - ((E) -3-pentafluorophenyl-2-propen-1-yl) -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 623 [M + H]⁺</li><li>(150) 1 - [(4-nitro-naphthalen-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.41 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 602 [M + H]⁺</li><li>(151) 1 - [(Benzooxazol-2-y) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] xanthine R_fValue: 0.40 (silica gel, cyclohexane / ethyl acetate = 3: 7) Mass Spectrum (ESI⁺): m / z = 548 [M + H]⁺</li><li>(152) 1 - [(5-nitrobenzooxazol-2-y) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.50 (silica gel, cyclohexane / ethyl acetate / methanol = 5: 4: 1) Mass Spectrum (ESI⁺): m / z = 593 [M + H]⁺</li><li>(153) 1 - [(3-Methyl-isoquinolin-1-yl) methyl] -3-methyl-7- (3-methyl-1-buten-1-yl) -8-bromo-xanthine R_fValue: 0.65 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 468, 470 [M + H]⁺</li><li>(154) 1 - [(quinolin-7-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] xanthine Mass Spectrum (ESI⁺): m / z = 558 [M + H]⁺</li><li>(155) 1 - [([1,5] -naphthyridin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine -1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 559 [M + H]⁺</li><li>(156) 1 - [(8-methyl-quinoxalin-6-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.45 (silica gel, methylene chloride / methanol = 19: 1) Mass Spectrum (ESI⁺): m / z = 573 [M + H]⁺</li><li>(157) 1 - [(2,3,8-trimethyl-quinoxalin-6-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.32 (silica gel, methylene chloride / methanol = 96: 4) Mass Spectrum (ESI⁺): m / z = 601 [M + H]⁺</li><li>(158) 1 - [([1,6] -naphthyridin-5-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine -1-yl] -xanthine R_fValue: 0.20 (silica gel, ethyl acetate / methanol = 98: 2) Mass Spectrum (ESI⁺): m / z = 559 [M + H]⁺</li><li>(159) 1 - [([1,8] Naphthyridin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine -1-yl] -xanthine R_fValue: 0.12 (silica gel, ethyl acetate / methanol = 98: 2) Mass Spectrum (ESI⁺): m / z = 559 [M + H]⁺</li><li>(160) 1 - [(4-Fluoro-naphthalen-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.47 (silica gel, petroleum ether / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 575 [M + H]⁺</li><li>(161) 1 - [([1,5] naphthyridin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.39 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 559 [M + H]⁺</li><li>(162) 1- [2- (3-methyl-2-oxo-2,3-dihydro-benzooxazol-4-yl) -2-oxo-ethyl] -3-methyl-7- (2-butyne-1 yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.60 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 606 [M + H]⁺</li><li>(163) 1 - [(8-phenylquinoxaline-6-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.48 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 356 [M + H]⁺</li><li>(164) 1 - [([1,5] -naphthyridin-4-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(R) -3- (tert. butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.25 (silica gel, ethyl acetate / petroleum ether = 4: 1) Mass Spectrum (ESI⁺): m / z = 559 [M + H]⁺</li><li>(165) 1 - ((E) -3-pentafluorophenyl-allyl) -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 623 [M + H]⁺</li><li>(166) 1 - [(E) -3- (2-trifluoromethylphenyl) allyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 601 [M + H]⁺</li><li>(167) 1 - [(E) -3- (3-trifluoromethylphenyl) allyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 601 [M + H]⁺</li><li>(168) 1 - [(E) -3- (4-trifluoromethylphenyl) allyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 601 [M + H]⁺</li><li>(169) 1 - [(3-trifluoromethyl-isoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.68 (silica gel, cyclohexane / ethyl acetate = 3: 7) Mass Spectrum (ESI⁺): m / z = 626 [M + H]⁺</li><li>(170) 1 - [(3-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-cyano-benzyl) -8-chlorxanthine</li><li>(171) 1 - [(3-Difluoromethylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.38 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 608 [M + H]⁺</li><li>(172) 1 - [(4-chloro-3-methoxyisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino ) piperidin-1-yl] -xanthine R_fValue: 0.65 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 622, 624 [M + H]⁺</li><li>(173) 1 - [(4-ethoxyquinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.25 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 603 [M + H]⁺</li><li>(174) 1 - [(4-isopropyloxyquinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.40 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 617 [M + H]⁺</li><li>(175) 1 - [(2-Methylbenzothiazol-6-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.56 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 578 [M + H]⁺</li><li>(176) 1 - [(3-phenylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.75 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 634 [M + H]⁺</li><li>(177) 1 - [(4-Phenyloxyquinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.35 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 651 [M + H]⁺</li><li>(178) 1 - [(4-phenyl-quinazolin-2-yl) methyl] -3-cyclopropyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine. 1-yl] -xanthine R_fValue: 0.45 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 661 [M + H]⁺</li><li>(179) 1 - [(3-Methylisoquinolin-1-yl) methyl] -3-cyclopropyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.50 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 598 [M + H]⁺</li><li>(180) 1- [2- (3-Difluoromethoxyphenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_f-W ert: 0.77 (silica gel, methylene chloride / Essigester = 1: 1) Mass Spectrum (ESI⁺): m / z = 601 [M + H]⁺</li><li>(181) 1 - [(2-phenylquinazolin-4-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.65 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 635 [M + H]⁺</li><li>(182) 1- [2- (2-Methoxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) piperidin-1-yl] -xanthine R_fValue: 0.57 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 565 [M + H]⁺</li><li>(183) 1- [2- (3-methoxyphenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) piperidin-1-yl] -xanthine R_fValue: 0.63 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 565 [M + H]⁺</li><li>(184) 1- [2- (3-trifluoromethoxyphenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.64 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 619 [M + H]⁺</li><li>(185) 1- [2- (biphenyl-2-yl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.70 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 611 [M + H]⁺</li><li>(186) 1- [2- (biphenyl-3-yl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.75 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 611 [M + H]⁺</li><li>(187) 1- [2- (3-isopropyloxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.66 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 593 [M + H]⁺</li><li>(188) 1 - [(3-Methylisoquinolin-1-yl) methyl] -3-cyclopropyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.50 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 598 [M + H]⁺</li><li>(189) 1 - [(4-phenylquinazolin-2-yl) methyl] -3-cyclopropyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.50 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 661 [M + H]⁺</li><li>(190) 1 - [(4-Cyano-naphthalen-1-yl) methyl] -3-cyclopropyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.75, (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 608 [M + H]⁺</li><li>(191) 1- [2- (2-phenyloxyphenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.85 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 627 [M + H]⁺</li><li>(192) 1- [2- (3-ethoxyphenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.72 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 579 [M + H]⁺</li><li>(193) 1- [2- (3-methoxyphenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.67 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 565 [M + H]⁺</li><li>(194) 1- [2- (2-methoxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl) -xanthine R_fValue: 0.57 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 565 [M + H]⁺</li><li>(195) 1 - [(3-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-chloro-benzyl) -8-bromxanthine</li><li>(196) 1 - [(3-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-bromo-benzyl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine</li><li>(197) 1 - [(1,2,3,4-tetrahydrophenanthridin-6-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert. -Butyloxycarbonylamino) piperidin-1-yl] -xanthine R_fValue: 0.55 (silica gel, ethyl acetate / petroleum ether = 2: 1) Mass Spectrum (ESI⁺): m / z = 612 [M + H]⁺</li></ul>

Example VI

1- (2- {3 - [(methanesulphinyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert-butyloxycarbonlyamino) piperidin-1-yl] -xanthine

0039To a solution of 402 mg of 1- (2- {3 - [(methylsulfanyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine in 10 ml of hexafluoroisopropanol are added 0.15 ml of a 35% hydrogen peroxide solution. The reaction mixture is stirred for half an hour at room temperature. Then 5 ml of a 10% sodium thiosulfate solution are added. The aqueous phase is extracted twice with 5 ml of methylene chloride each time. The combined extracts are dried over sodium sulfate and concentrated. The yellow residue is purified by chromatography on a silica gel column with cyclohexane / ethyl acetate / methanol (5: 4: 1) as eluent. Yield: 299 mg (73% of theory) R_fValue: 0.28 (silica gel, cyclohexane / ethyl acetate / methanol = 5: 4: 1) Mass Spectrum (ESI⁺): m / z = 643 [M + H]⁺

0040The following compounds are obtained analogously to Example VI:<ol id="ol0007"><li>(1) 1- [2- (3-Methanesulfinyl-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert .-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.05 (silica gel, ethyl acetate / cyclohexane = 3: 1) Mass Spectrum (ESI⁺): m / z = 613 [M + H]⁺</li><li>(2) 1- (2- {2 - [(methanesulfinyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8- [3- ( tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 627 [M + H]⁺</li></ol>

Example VII

3 - [(2-trimethylsilanyl-ethoxy) methyl] -7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine

0041To 630 mg of 7- (3-methyl-2-buten-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine in 11 ml of acetonitrile are added 236 μl of 1,8- Diazabicyclo [5.4.0] undec-7-ene dropped. The solution is stirred for two hours at room temperature, then the acetonitrile is distilled off in vacuo. The flask residue is taken up in 11 ml of N, N-dimethylformamide and treated with 258 mg of (2-trimethylsilanyl-ethoxy) methyl chloride. The reaction mixture is stirred for three hours at 120.degree. For workup, water is added, the precipitate filtered off and taken up in ethyl acetate. The solution is dried over magnesium sulfate, concentrated and chromatographed on a silica gel column with cyclohexane / ethyl acetate / methanol (6: 1: 0 to 0: 5: 1) as the eluent. Yield: 435 mg (53% of theory) Mass Spectrum (ESI⁺): m / z = 549 [M + H]⁺

0042The following compounds are obtained analogously to Example VII:<ol id="ol0008"><li>(1) 3 - [(2-Trimethylsilanyl-ethoxy) methyl] -7- (2-cyano-benzyl) -xanthine Mass Spectrum (ESI^-): m / z = 396 [MH]^-</li><li>(2) 3 - [(Methoxycarbonyl) methyl] -7- (3-methyl-2-buten-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.31 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 491 [M + H]⁺</li></ol>

Example VIII

7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine

0043To 2.32 g of 2- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -3- (3-methyl-2-buten-1-yl) -4-ethoxycarbonyl-5 - {[(ethoxycarbonylamino) carbonyl ] amino} -3<i>H</i>imidazole in 35 ml of ethanol is added 510 mg of potassium tert-butoxide. The yellow solution is refluxed for five hours. After cooling to room temperature, it is diluted with methylene chloride. The organic phase is washed with saturated ammonium chloride solution and saturated sodium chloride solution, dried over magnesium sulfate and concentrated. The crude product is chromatographed on a silica gel column with methylene chloride / methanol / conc. methanolic ammonia (95: 5: 1 to 90: 10: 1) as the eluent. Yield: 630 mg (35% of theory) R_fValue: 0.24 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 419 [M + H]⁺

Example IX

2- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -3- (3-methyl-2-buten-1-yl) -4-ethoxycarbonyl-5 - {[(ethoxycarbonylamino) carbonyl] amino} -3<i>H</i>imidazole

0044To 4.00 g of 2- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -3- (3-methyl-2-buten-1-yl) -4-ethoxycarbonyl-5-amino-3H-imidazole in 90 ml of 1,2-dimethoxyethane 2.97 ml of Isocanatameisensäureethylester are added and the light brown solution is heated overnight at 120 ° C in an oil bath. Then another 0.6 ml Isocanatameisensäureethylester are added and it is heated for another four hours. For workup, the reaction mixture is mixed with saturated potassium carbonate solution and extracted with ethyl acetate. The organic phase is dried over magnesium sulfate, concentrated by evaporation and through a silica gel column with methylene chloride / methanol / conc. methanolic ammonia (98: 2: 1 to 90: 10: 1) as the eluent. Yield: 2.27 g (45% of theory) R_fValue: 0.29 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 537 [M + H]⁺

Example X

2- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -3- (3-methyl-2-buten-1-yl) -4-ethoxycarbonyl-5-amino-3<i>H</i>imidazole

0045prepared by reacting cyanimino [N- (3-methyl-2-buten-1-yl) -N- (ethoxycarbonylmethyl) -amino] - [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -methane with sodium in ethanol at reflux. R_fValue: 0.26 (alumina, ethyl acetate / petroleum ether = 8: 2) Mass Spectrum (ESI⁺): m / z = 422 [M + H]⁺

Example XI

Cyanimino- [N- (3-methyl-2-buten-1-yl) -N- (ethoxycarbonylmethyl) amino] - [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -methane

0046prepared by reacting cyanimino [N- (3-methyl-2-buten-1-yl) -N- (ethoxycarbonylmethyl) -amino] -phenyloxy-methane with 3- (tert-butyloxycarbonylamino) -piperidine in the presence of potassium carbonate in N, N-dimethylformamide at room temperature. R_fValue: 0.10 (silica gel, petroleum ether / ethyl acetate = 6: 4) Mass Spectrum (ESI⁺): m / z = 422 [M + H]⁺

Example XII

Cyanimino- [N- (3-methyl-2-buten-1-yl) -N- (ethoxycarbonylmethyl) amino] -phenyloxy-methane

0047prepared by reacting cyanimino - [(ethoxycarbonylmethyl) amino] -phenyloxy-methane with 1-bromo-3-methyl-2-butene in the presence of potassium carbonate in acetone at room temperature. R_fValue: 0.70 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 316 [M + H]⁺

Example XIII

Cyanoimino - [(ethoxycarbonylmethyl) amino] -phenyloxy-methane

0048prepared by reacting Diphenylcyanocarbonimidat with Aminoessigsäureethylester hydrochloride in the presence of triethylamine in isopropanol at room temperature (analog <nplcit id="ncit0004" npl-type="s"><text>R. Besse et al., Tetrahedron 1990, 46, 7803-7812</text></nplcit>). R_fValue: 0.73 (silica gel, petroleum ether / ethyl acetate = 8: 2) Mass Spectrum (ESI⁺): m / z = 248 [M + H]⁺

Example XIV

1-Methyl-3 - [(methoxycarbonyl) methyl] -7- (2-cyano-benzyl) -8-chloro-xanthine

0049prepared by reacting 1-methyl-7- (2-cyano-benzyl) -8-chloro-xanthine with methyl bromoacetate in the presence of potassium carbonate in N, N-dimethylformamide at room temperature. R_fValue: 0.80 (silica gel, methylene chloride / methanol = 9: 1) Mass Spectrum (ESI⁺): m / z = 388, 390 [M + H]⁺

0050The following compounds are obtained analogously to Example XIV:<ol id="ol0009"><li>(1) 1-Methyl-3-cyanomethyl-7- (2-cyano-benzyl) -8-chloro-xanthine Mass Spectrum (ESI⁺): m / z = 355, 357 [M + H]⁺</li><li>(2) 1-Methyl-3- (2-propyn-1-yl) -7- (2-cyano-benzyl) -8-chloro-xanthine R_fValue: 0.80 (silica gel, methylene chloride / methanol <b>=</b> 95: 5) Mass Spectrum (ESI⁺): m / z = 354, 356 [M + H]⁺</li><li>(3) 1-Methyl-3- (2-propen-1-yl) -7- (2-cyano-benzyl) -8-chloro-xanthine R_fValue: 0.90 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 356, 358 [M + H]⁺</li><li>(4) 1- (2-Phenyl-2-oxo-ethyl) -3-cyanomethyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidine -1-yl] -xanthine R_fValue: 0.78 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 576 [M + H]⁺</li><li>(5) 1-Methyl-3-isopropyl-7- (2-cyano-benzyl) -8-chloro-xanthine Mass Spectrum (ESI⁺): m / z = 358, 360 [M + H]⁺</li></ol>

Example XV

1-Methyl-7- (2-cyano-benzyl) -8-chloro-xanthine

0051prepared by treating 1-methyl-3 - [(2-trimethylsilanylethoxy) methyl] -7- (2-cyanobenzyl) -8-chloro-xanthine with trifluoroacetic acid in methylene chloride at room temperature. R_fValue: 0.50 (silica gel, methylene chloride / methanol = 9: 1) Mass Spectrum (ESI⁺): m / z = 316, 318 [M + H]⁺

0052The following compounds are obtained analogously to Example XV:<ol id="ol0010"><li>(1) 1- (2-Phenyl-2-oxo-ethyl) -3-methyl-8-bromo-xanthine R_fValue: 0.26 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI^-): m / z = 361, 363 [MH]^-</li><li>(2) 1 - [(4-Oxo-3,4-dihydro-phthalazin-1-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- (3 -amino-piperidin-1-yl) -xanthine (Since the compound still contains impurities that can not be removed chromatographically, the material is transferred again into the BOC-protected derivative and then purified by chromatography, see Example XXV (1).) Mass Spectrum (ESI⁺): m / z = 491 [M + H]⁺</li></ol>

Example XVI

1-Methyl-3 - [(2-trimethylsilanyl-ethoxy) methyl] -7- (2-cyano-benzyl) -8-chloro-xanthine

0053prepared by chlorination of 1-methyl-3 - [(2-trimethylsilanyl-ethoxy) methyl] -7- (2-cyano-benzyl) -xanthine with N-chlorosuccinimide in dichloroethane under reflux. Mass spectrum (EI): m / z = 445, 447 [M]⁺

Example XVII

7- (2-cyano-benzyl) -xanthine

0054prepared by treating 16.68 g of 2-amino-7- (2-cyano-benzyl) -1,7-dihydropurin-6-one with 17.00 g of sodium nitrite in a mixture of 375 ml of conc. Acetic acid, 84 ml of water and 5.2 ml of conc. Hydrochloric acid at 50 ° C. Yield: 8.46 g (50% of theory) Mass Spectrum (ESI⁺): m / z = 268 [M + H]⁺

Example XVIII

(2-cyano-benzyl) -1,7-dihydro-purin-6-one 2-Amino-7-

0055prepared by reacting 20.00 g of guanosine hydrate with 22.54 g of 2-cyanobenzyl bromide in dimethyl sulfoxide at 60 ° C and subsequent treatment with 57 ml of conc. Hydrochloric acid. Yield: 18.00 g (97% of theory) Mass Spectrum (ESI⁺): m / z = 267 [M + H]⁺

Example XIX

1- {2- [3- (2-oxo-imidazolidin-1-yl) phenyl] -2-oxo-ethyl} -3-methyl-7- (3-methyl-2-buten-1-yl) - 8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine

0056prepared by treating 1- [2- (3 - {[(2-chloroethylamino) carbonyl] amino} phenyl) -2-oxoethyl] -3-methyl-7- (3-methyl-2-butene 1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine with potassium tert -butylate in N, N-dimethylformamide at room temperature. R_fValue: 0.50 (silica gel, methylene chloride / methanol = 9: 1)

Example XX

1- [2- (3 - {[(2-chloro-ethylamino) carbonyl] amino} phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl ) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine

0057prepared by reacting 221 mg of 1- [2- (3-amino-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3 - (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine with 60 ul of 2-chloroethyl isocyanate in 3 ml of methylene chloride at room temperature. Yield: 163 mg (64% of theory) R_fValue: 0.20 (silica gel, cyclohexane / ethyl acetate / methanol = 6: 3: 1) Mass Spectrum (ESI⁺): m / z = 671, 673 [M + H]⁺

0058The following compounds are obtained analogously to Example XX:<ol id="ol0011" compact="compact"><li>(1) 1- [2- (2 - {[(ethoxycarbonylamino) carbonyl] amino} phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Carrying out in N, N-dimethylformamide at 30 ° C.) R_fValue: 0.26 (silica gel, cyclohexane / ethyl acetate = 4: 6) Mass Spectrum (ESI⁺): m / z = 681 [M + H]⁺</li></ol>

Example XXI

1- [2- (3-Amino-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino ) piperidin-1-yl] -xanthine

0059prepared by treating 1- [2- (3-nitro-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- ( tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine with iron powder in a mixture of ethanol, water and glacial acetic acid (80:25:10) at 100 ° C. R_fValue: 0.55 (silica gel, cyclohexane / ethyl acetate / methanol / concentrated aqueous ammonia = 50: 30: 20: 1) Mass Spectrum (ESI⁺): m / z = 566 [M + H]⁺

0060The following compounds are obtained analogously to Example XXI:<ol id="ol0012"><li>(1) 1- [2- (2-Amino-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert .-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 566 [M + H]⁺</li><li>(2) 1- [2- (2-Amino-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8 - [(S) - 3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 566 [M + H]⁺</li><li>(3) 1 - [(5-Aminoisoquinolin-1-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert-butyloxycarbonylamino ) piperidin-1-yl] -xanthine R_fValue: 0.22 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 589 [M + H]⁺</li><li>(4) 1- [2- (2-Amino-phenyl) -2-oxo-ethyl] -3-methyl-7 - [(1-cyclopenten-1-yl) methyl] -8-bromo-xanthine Mass Spectrum (ESI⁺): m / z = 458, 460 [M + H]⁺</li><li>(5) 1- [2- (2-Amino-phenyl) -2-oxo-ethyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8-bromo-xanthine (Product contains about 10% Z-isomer) R_fValue: 0.55 (silica gel, cyclohexane / ethyl acetate = 4: 6) Mass Spectrum (ESI⁺): m / z = 432, 434 [M + H]⁺</li><li>(6) 1- [2- (2-Amino-phenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8-bromo-xanthine R_fValue: 0.50 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 430, 432 [M + H]⁺</li><li>(7) 1- [2- (2-Amino-phenyl) -2-oxo-ethyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 552 [M + H]⁺</li><li>(8) 1- [2- (2-Amino-phenyl) -2-oxo-ethyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 552 [M + H]⁺</li><li>(9) 1- [2- (2-Amino-3-methoxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- 3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.82 (silica gel, ethyl acetate / petroleum ether = 4: 1) Mass Spectrum (ESI⁺): m / z = 596 [M + H]⁺</li></ol>

Example XXII

1- (2- {2 - [(ethylcarbonyl) amino] phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine

0061prepared by reacting 248 mg of 1- [2- (2-amino-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3 - (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine with 40 ul propionyl chloride in the presence of 60 ul pyridine in N, N-dimethylformamide at 80 ° C. Yield: 168 mg (62% of theory) R_fValue: 0.55 (silica gel, cyclohexane / ethyl acetate = 3: 7) Mass Spectrum (ESI⁺): m / z = 622 [M + H]⁺

0062The following compounds are obtained analogously to Example XXII:<ol id="ol0013"><li>(1) 1 - ({5 - [(Methoxycarbonyl) methylamino] -isoquinolin-1-yl} methyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3 (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Carrying out with methyl bromoacetate and potassium carbonate) R_fValue: 0.42 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 661 [M + H]⁺</li><li>(2) 1- [2- (2-Acetylamino-phenyl) -2-oxo-ethyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8- [3- (tert .-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Product contains about 10% Z-isomer) Mass Spectrum (ESI⁺): m / z = 594 [M + H]⁺</li><li>(3) 1- (2- {2 - [(isopropylcarbonyl) amino] -phenyl} -2-oxo-ethyl) -3-methyl-7 - ((E) -2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Product contains about 10% Z-isomer) Mass Spectrum (ESI⁺): m / z = 622 [M + H]⁺</li><li>(4) 1- [2- (2-acetylamino-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8 - [(<i>S</i>) - 3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.50 (silica gel, cyclohexane / ethyl acetate = 3: 7) Mass Spectrum (ESI⁺): m / z = 608 [M + H]⁺</li><li>(5) 1- [2- (2-Acetylamino-phenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert-butyloxycarbonylamino) piperidin-1-yl] -xanthine R_fValue: 0.34 (silica gel, cyclohexane / ethyl acetate = 3: 7) Mass Spectrum (ESI⁺): m / z = 592 [M + H]⁺</li><li>(6) 1- (2- {2 - [(isopropylcarbonyl) amino] -phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.25 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 636 [M + H]⁺</li><li>(7) 1- (2- {2 - [(isopropylcarbonyl) amino] -phenyl} -2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8- [3- ( tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.44 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 620 [M + H]⁺</li><li>(8) 1- [2- (2-Acetylamino-phenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(S) -3- (tert .-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.34 (silica gel, cyclohexane / ethyl acetate = 3: 7) Mass Spectrum (ESI⁺): m / z = 592 [M + H]⁺</li><li>(9) 1- (2- {2 - [(isopropylcarbonyl) amino] -phenyl} -2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.44 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 620 [M + H]⁺</li><li>(10) 1- (2- {2 - [(Methoxycarbonyl) amino] -phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Carrying out in acetonitrile at 55 ° C) R_fValue: 0.25 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 624 [M + H]⁺</li><li>(11) 1- (2- {2 - [(isopropylcarbonyl) amino] -phenyl} -2-oxo-ethyl) -3-methyl-7 - ((E) -2-buten-1-yl) -8- [(S) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Carried out in acetonitrile at 65 ° C) R_fValue: 0.50 (silica gel, cyclohexane / ethyl acetate / isopropanol = 14: 3: 3) Mass Spectrum (ESI⁺): m / z = 622 [M + H]⁺</li><li>(12) 1- (2- {2 - [(ethylcarbonyl) amino] -phenyl} -2-oxo-ethyl) -3-methyl-7 - ((E) -2-buten-1-yl) -8- [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 608 [M + H]⁺</li><li>(13) 1- [2- (2-Acetylamino-phenyl) -2-oxo-ethyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 594 [M + H]⁺</li><li>(14) 1- [2- (2-acetylamino-phenyl) -2-oxo-ethyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - [(<i>S</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.28 (silica gel, cyclohexane / ethyl acetate / isopropanol = 8: 1: 1) Mass Spectrum (ESI⁺): m / z = 594 [M + H]⁺</li><li>(15) 1- (2- {2 - [(isopropylcarbonyl) amino] -phenyl} -2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.90 (silica gel, methylene chloride / methanol = 9: 1)</li><li>(16) 1- (2- {2 - [(isopropylcarbonyl) amino] -phenyl} -2-oxo-ethyl) -3-methyl-7 - ((E) -2-buten-1-yl) -8- [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl]) - xanthine (Carrying out in 1,2-dichloroethane at 45 ° C) R_fValue: 0.30 (silica gel, cyclohexane / ethyl acetate / isopropanol = 8: 1: 1) Mass Spectrum (ESI⁺): m / z = 622 [M + H]⁺</li><li>(17) 1- (2- {2 - [(ethylcarbonyl) amino] -phenyl} -2-oxo-ethyl) -3-methyl-7 - ((E) -2-buten-1-yl) -8- [(S) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.48 (silica gel, cyclohexane / ethyl acetate / isopropanol = 14: 3: 3) Mass Spectrum (ESI⁺): m / z = 608 [M + H]⁺</li><li>(18) 1- (2- {2 - [(ethylcarbonyl) amino] phenyl} -2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 606 [M + H]⁺</li><li>(19) 1- (2- {2 - [(ethylcarbonyl) amino] -phenyl} -2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8 - [(S) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.22 (silica gel, methylene chloride / methanol = 95: 5)</li><li>(20) 1- (2- {2 - [(phenylcarbonyl) amino] -phenyl} -2-oxo-ethyl) -3-methyl-7 - ((E) -2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.55 (silica gel, cyclohexane / ethyl acetate / isopropanol = 14: 3: 3) Mass Spectrum (ESI⁺): m / z = 656 [M + H]⁺</li><li>(21) 1- (2- {2 - [(Cyclopropylcarbonyl) amino] phenyl} -2-oxo-ethyl) -3-methyl-7 - [(1-cyclopenten-1-yl) methyl] -8- [ 3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Carrying out with Hünigbase and 4-dimethylaminopyridine in methylene chloride) R_fValue: 0.60 (silica gel, methylene chloride / methanol = 18: 1)</li></ol>

Example XXIII

1- (2- {3 - [(methoxycarbonyl) methoxy] phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- (3- amino-piperidin-1-yl) -xanthine

0063prepared by treating 1- (2- {3 - [(methoxycarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8 - [3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine with trifluoroacetic acid in methylene chloride at room temperature. Mass Spectrum (ESI⁺): m / z = 539 [M + H]⁺

0064The following compounds are obtained analogously to Example XXIII:<ol id="ol0014" compact="compact"><li>(1) 1- (2- {2 - [(Methoxycarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- (3-amino-piperidin-1-yl) -xanthine Mass Spectrum (ESI⁺): m / z = 539 [M + H]⁺</li></ol>

Example XXIV

1-methyl-3-phenyl-7- (2-cyano-benzyl) -8-chloro-xanthine

0065A mixture of 829 mg of 1-methyl-7- (2-cyano-benzyl) -8-chloro-xanthine, 640 mg of phenylboronic acid, 509 mg of anhydrous copper acetate and 0.43 ml of pyridine in 20 ml of methylene chloride becomes 4Å in the presence of 100 mg of molecular sieve Stirred at room temperature for days. Then another 320 mg phenylboronic acid are added and the reaction mixture is stirred for a further day at room temperature. For workup, the mixture is filtered through talc and washed with ethyl acetate. The filtrate is concentrated and chromatographed on a silica gel column with cyclohexane / ethyl acetate (7: 3 to 1: 1) as the eluent. Yield: 142 mg (14% of theory) Mass Spectrum (ESI⁺): m / z = 392, 394 [M + H]⁺

Example XXV

1- (2-phenyl-2-oxo-ethyl) -7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine

0066prepared by reacting 1- (2-phenyl-2-oxo-ethyl) -7- (3-methyl-2-buten-1-yl) -8- (3-amino-piperidin-1-yl) -xanthine with Pyrocarbonic acid di-tert-butyl ester in the presence of Hünigbase in methylene chloride at room temperature. R_fValue: 0.27 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1)

0067The following compounds are obtained analogously to Example XXV:<ol id="ol0015"><li>(1) 1 - [(4-Oxo-3,4-dihydro-phthalazin-1-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3 - (tert-butyloxycarbonyl-amino) piperidin-1-yl] -xanthine R_fValue: 0.27 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 591 [M + H]⁺</li><li>(2) 7-Acetyl-1- (tert-butyloxycarbonyl) -1H-indole R_fValue: 0.82 (silica gel, methylene chloride / petroleum ether / ethyl acetate = 5: 4: 1) Mass Spectrum (ESI⁺): m / z = 260 [M + H]⁺</li></ol>

Example XXVI

1 - [(cinnolin-4-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8-chloro-xanthine and 1 - [(1,4-dihydro-cinnoline -4-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8-chloro-xanthine

0068To 830 mg of 3-methyl-7- (3-methyl-2-buten-1-yl) -8-chloro-xanthine and 1.25 g of triphenylphosphine in 25 ml of tetrahydrofuran are added 510 mg of a mixture of (cinnolin-4-yl) - methanol and (1,4-dihydro-cinnolin-4-yl) -methanol (see Example XXVII). The reaction mixture is treated with 0.92 ml of diethyl azodicarboxylate and stirred overnight at room temperature. It is then concentrated and chromatographed on a silica gel column with ethyl acetate / petroleum ether (7: 3 to 0: 1) as the eluent. A mixture of cinnoline and 1,4-dihydro-cinnoline compound is obtained. Amount: 660 mg (52% of theory) R_fValue: 0.60 (silica gel, ethyl acetate / petroleum ether = 7: 3)

0069The following compounds are obtained analogously to Example XXVI:<ol id="ol0016"><li>(1) 1 - ({4-Oxo-3 - [(2-trimethylsilanylethoxy) methyl] -3,4-dihydro-phthalazin-1-yl} methyl) -3-methyl-7- (3-methyl) 2-buten-1-yl) -8-chloro-xanthine R_fValue: 0.85 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 557, 559 [M + H]⁺</li><li>(2) 1 - [(isoquinolin-3-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8-chloro-xanthine Melting point: 194-195 ° C Mass Spectrum (ESI⁺): m / z = 410, 412 [M + H]⁺</li><li>(3) 1 - [(3-Methyl-4-oxo-3,4-dihydro-phthalazin-1-yl) methyl] -3-methyl-7- (3-methyl-2-buten-1-yl) - 8-chloro-xanthine R_fValue: 0.66 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 441, 443 [M + H]⁺</li><li>(4) 1 - [(Quinolin-4-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8-bromo-xanthine (Carrying out with potassium carbonate) R_fValue: 0.45 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 438, 440 [M + H]⁺</li><li>(5) 1 - [(isoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8-bromo-xanthine R_fValue: 0.78 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 438, 440 [M + H]⁺</li><li>(6) 1 - [(4-Dimethylamino-naphthalen-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidine 1-yl] -xanthine R_fValue: 0.80 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 600 [M + H]⁺</li><li>(7) 1 - [(isoquinolin-1-yl) methyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8-bromo-xanthine (The product contains about 20% Z-isomer) R_fValue: 0.71 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 440, 442 [M + H]⁺</li><li>(8) 1 - [(1-methyl-1<i>H</i>indol-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8-bromo-xanthine R_fValue: 0.95 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 440, 442 [M + H]⁺</li><li>(9) 1 - [(Quinolin-3-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8-bromo-xanthine R_fValue: 0.55 (silica gel, ethyl acetate / petroleum ether = 8: 2) Mass Spectrum (ESI⁺): m / z = 438, 440 [M + H]⁺</li><li>(10) 1 - {[1- (tert-Butyloxycarbonylamino) -1<i>H</i>indol-2-yl] methyl} -3-methyl-7- (2-butyn-1-yl) -8-bromo-xanthine R_fValue: 0.74 (silica gel, petroleum ether / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 526, 528 [M + H]⁺</li><li>(11) 1 - ({2-Methyl-1 - [(2-trimethylsilanylethoxy) methyl] -1<i>H</i>-benzoimidazol-5-yl} methyl) -3-methyl-7- (2-butyn-1-yl) -8-bromo-xanthine (in admixture with 1- ({2-methyl-3 - [(2-trimethylsilanyl ethoxy) methyl] -3<i>H</i>-benzoimidazol-5-yl} methyl) -3-methyl-7- (2-butyn-1-yl) -8-bromo-xanthine) Mass Spectrum (ESI⁺): m / z = 571, 573 [M + H]⁺</li><li>(12) 1 - [(1 - [(2-trimethylsilanylethoxy) methyl] -1<i>H</i>benzoimidazol-5-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8-bromo-xanthine (in admixture with 1 - [(3 - [(2-trimethylsilanyl-ethoxy) -methyl ] -3<i>H</i>-benzoimidazol-5-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8-bromoxanthine) R_fValue: 0.50 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 557, 559 [M + H]⁺</li><li>(13) 1 - [(pyrazolo [1,5-a] pyridin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8-bromo-xanthine R_fValue: 0.35 (silica gel, petroleum ether / ethyl acetate = 1: 2) Mass Spectrum (ESI⁺): m / z = 427, 429 [M + H]⁺</li></ol>

Example XXVII

(Cinnolin-4-yl) -methanol and (1,4-dihydro-cinnolin-4-yl) -methanol

0070A solution of 1.00 g of methyl cinnoline-4-carboxylate in 15 ml of diethyl ether is added dropwise at 0 ° C to a suspension of 222 mg of lithium aluminum hydride in 5 ml of diethyl ether. After 1.5 hours, the reaction mixture is carefully added dropwise with water, stirred with methylene chloride and filtered with suction through a glass fiber filter. The aqueous phase is extracted with methylene chloride and the combined organic phases are dried over magnesium sulfate and concentrated. Loud¹H-NMR is a mixture of cinnoline and 1,4-dihydro-cinnoline compound obtained as a yellow oil, which is reacted further without further purification. Amount: 530 mg (62% of theory) R_fValue: 0.63 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 161 [M1 + H]⁺ and 163 [M2 + H]⁺

0071The following compounds are obtained analogously to Example XXVII:<ol id="ol0017"><li>(1) {2-Methyl-1 - [(2-trimethylsilanylethoxy) methyl] -1<i>H</i>benzoimidazol-5-yl) -methanol (in admixture with {2-methyl-3 - [(2-trimethylsilanylethoxy) methyl] -3<i>H</i>-benzoimidazol-5-yl} methanol) Mass Spectrum (ESI⁺): m / z = 293 [M + H]⁺</li><li>(2) (2,3,8-trimethyl-quinoxalin-6-yl) -methanol R_fValue: 0.45 (silica gel, petroleum ether / ethyl acetate = 1: 2) Mass Spectrum (ESI⁺): m / z = 203 [M + H]⁺</li><li>(3) (8-methyl-quinoxalin-6-yl) -methanol R_fValue: 0.18 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 175 [M + H]⁺</li><li>(4) (E) -3-pentafluorophenyl-2-propen-1-ol (Carrying out with diisobutylaluminum hydride in toluene) Mass spectrum (EI): m / z = 224 [M]⁺</li><li>(5) (E) -3- (2-trifluoromethylphenyl) -2-propen-1-ol (Carrying out with diisobutylaluminum hydride in toluene)</li><li>(6) (E) -3- (3-trifluoromethylphenyl) -2-propen-1-ol (Carrying out with diisobutylaluminum hydride in toluene) Mass spectrum (EI): m / z = 202 [M]⁺</li><li>(7) (E) -3- (4-trifluoromethyl-phenyl) -2-propen-1-ol (Carrying out with diisobutylaluminum hydride in toluene)</li></ol>

Example XXVIII

4-hydroxymethyl-2 - [(2-trimethylsilanyl-ethoxy) methyl] -2<i>H</i>phthalazin-1-one

0072prepared by treating methyl 4-oxo-3 - [(2-trimethylsilanylethoxy) methyl] -3,4-dihydro-phthalazine-1-carboxylate with sodium borohydride in tetrahydrofuran at 40 ° C. R_fValue: 0.55 (silica gel, cyclohexane / ethyl acetate 1: 1) Mass Spectrum (ESI⁺): m / z = 307 [M + H]⁺

0073The following compounds are obtained analogously to Example XXVIII:<ol id="ol0018"><li>(1) (3,4-Dimethyl-isoquinolin-1-yl) -methanol (Carrying out with lithium borohydride in tetrahydrofuran) R_fValue: 0.35 (silica gel, petroleum ether / ethyl acetate = 2: 1) Mass Spectrum (ESI⁺): m / z = 188 [M + H]⁺</li><li>(2) (3-Methylimidazo [1,2-a] pyridin-2-yl) -methanol (Carrying out with lithium borohydride in tetrahydrofuran) R_fValue: 0.48 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 163 [M + H]⁺</li><li>(3) (3,4-dimethyl-6,7-dihydro-5<i>H</i>- [2] pyrindin-1-yl) -methanol (Carrying out with lithium borohydride in tetrahydrofuran) R_fValue: 0.40 (alumina, petroleum ether / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 178 [M + H]⁺</li><li>(4) (3,4-dimethyl-5,6,7,8-tetrahydro-isoquinolin-1-yl) -methanol (Carrying out with lithium borohydride in tetrahydrofuran) R_fValue: 0.45 (alumina, petroleum ether / ethyl acetate = 3: 1) Mass Spectrum (ESI⁺): m / z = 192 [M + H]⁺</li><li>(5) 6-hydroxymethyl-1,2,3,4-tetrahydrophenanthridine (Carrying out with lithium borohydride in tetrahydrofuran at room temperature) R_fValue: 0.40 (silica gel, petroleum ether / ethyl acetate = 2: 1) Mass Spectrum (ESI⁺): m / z = 214 [M + H]⁺</li></ol>

Example XXIX

4-oxo-3 - [(2-trimethylsilanyl-ethoxy) methyl] -3,4-dihydro-phthalazin-1-carbonsäuremethylester

0074prepared by reaction of 4-oxo-3,4-dihydro-phthalazine-1-carboxylic acid methyl ester with (2-trimethylsilanyl-ethoxy) methyl chloride in the presence of Hünigbase in methylene chloride at room temperature. R_fValue: 0.75 (silica gel, cyclohexane / ethyl acetate 6: 4) Mass Spectrum (ESI⁺): m / z = 335 [M + H]⁺

0075The following compounds are obtained analogously to Example XXIX:<ol id="ol0019"><li>(1) 7-Acetyl-3 - [(2-trimethylsilanylethoxy) methyl] -3<i>H</i>-benzooxazol-2-one Mass Spectrum (ESI⁺): m / z = 308 [M + H]⁺</li><li>(2) 4-acetyl-3 - [(2-trimethylsilanylethoxy) methyl] -3<i>H</i>-benzooxazol-2-one R_fValue: 0.87 (silica gel, methylene chloride / methanol = 99: 1)</li><li>(3) 4-Acetyl-1,3-bis - [(2-trimethylsilanylethoxy) methyl] -1,3-dihydrobenzoimidazol-2-one (Carrying out with potassium tert-butoxide in N, N-dimethylformamide) R_fValue: 0.90 (silica gel, petroleum ether / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 437 [M + H]⁺</li><li>(4) 6-Methyl-1 - [(2-trimethylsilanylethoxy) methyl] -1<i>H</i>quinoline-2-one R_fValue: 0.78 (silica gel, petroleum ether / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 290 [M + H]⁺</li><li>(5) {2-Methyl-1 - [(2-trimethylsilanylethoxy) methyl] -1<i>H</i>benzoimidazol-5-yl} -carboxylic acid methyl ester (in admixture with {2-methyl-3 - [(2-trimethylsilanyl-ethoxy) methyl] -3<i>H</i>-benzoimidazol-5-yl} -carboxylic acid methyl ester) Mass Spectrum (ESI⁺): m / z = 321 [M + H]⁺</li></ol>

Example XXX

1- [2- (3-Methanesulfonyl-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino ) piperidin-1-yl] -xanthine

0076To 500 mg of 1- [2- (3-methylsulfanyl-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert .-Butyloxycarbonylamino) -piperidin-1-yl] -xanthine in 5 ml of methylene chloride are added 0.22 ml of a 35% hydrogen peroxide solution and 20 mg of sodium tungstate. The reaction mixture is stirred overnight at room temperature, then 1 ml of methanol is added. After a further 48 hours, another 1.5 ml of 35% hydrogen peroxide solution, a spatula tip of sodium tungstate and two drops of water are added. The next morning the oxidation according to thin layer chromatography is complete and the reaction mixture is diluted with 50 ml of methylene chloride and washed twice with 30 ml of 10% sodium thiosulfate solution. The organic phase is dried over magnesium sulfate and concentrated to leave a tough resin, Yield: 530 mg (100% of theory) R_fValue: 0.72 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 629 [M + H]⁺

Example XXXI

1- [2- (3-carboxy-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino ) piperidin-1-yl] -xanthine

0077prepared by treating 1- [2- (3-methoxycarbonyl-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- ( tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine with 3 M sodium hydroxide solution in methanol at room temperature. R_fValue: 0.34 (silica gel, methylene chloride / methanol = 9: 1) Mass Spectrum (ESI⁺): m / z = 595 [M + H]⁺

0078Analogously to Example XXXI, the following compounds are obtained:<ol id="ol0020"><li>(1) 1- [2- (2-carboxyphenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert .-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.49 (silica gel, methylene chloride / methanol = 9: 1)</li><li>(2) 1- [2- (2-carboxymethoxyphenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) piperidin-1-yl] -xanthine (Carrying out with 4 M potassium hydroxide solution in tetrahydrofuran) Mass Spectrum (ESI⁺): m / z = 609 [M + H]⁺</li><li>(3) 1- [2- (2-Carboxymethylamino-phenyl) -2-oxo-ethyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Carrying out with 4 M potassium hydroxide solution in tetrahydrofuran) R_fValue: 0.65 (silica gel, cyclohexane / ethyl acetate = 3: 7) Mass Spectrum (ESI⁺): m / z = 610 [M + H]⁺</li><li>(4) 1-Carboxymethyl-3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 475 [M + H]⁺</li></ol>

Example XXXII

1- {2- [3- (methylaminocarbonyl) -phenyl] -2-oxo-ethyl} -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert. -Butyloxycarbonylamino) piperidin-1-yl] -xanthine

0079A mixture of 190 mg of 1- [2- (3-carboxyphenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine, 43 μl of a 40% aqueous methylamine solution, 103 mg of O- (benzotriazol-1-yl) -N, N, N ', N'-tetramethyluronium tetrafluoroborate , 43 mg of N-hydroxybenzotriazole and 45 ul of triethylamine in 3 ml of tetrahydrofuran is stirred for eight hours at room temperature. For workup, the reaction mixture is diluted with ethyl acetate and washed with water, 10% citric acid solution, 10% potassium carbonate solution and saturated sodium chloride solution. The organic phase is concentrated and chromatographed on a silica gel column with methylene chloride / methanol (98: 2 to 80:20) as the eluent. Yield: 173 mg (89% of theory) R_fValue: 0.30 (silica gel, methylene chloride / methanol = 20: 1) Mass Spectrum (ESI⁺): m / z = 608 [M + H]⁺

0080Analogously to Example XXXII, the following compounds are obtained:<ol id="ol0021"><li>(1) 1- {2- [3- (Dimethylaminocarbonyl) -phenyl] -2-oxo-ethyl} -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3 (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.28 (silica gel, methylene chloride / methanol = 20: 1) Mass Spectrum (ESI⁺): m / z = 622 [M + H]⁺</li><li>(2) 1- {2- [3- (morpholin-4-yl-carbonyl) -phenyl] -2-oxo-ethyl} -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.30 (silica gel, methylene chloride / methanol = 20: 1) Mass Spectrum (ESI⁺): m / z = 664 [M + H]⁺</li><li>(3) 1- {2- [2- (Dimethylaminocarbonyl) -phenyl] -2-oxo-ethyl} -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3 (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.30 (silica gel, methylene chloride / methanol = 20: 1) Mass Spectrum (ESI⁺): m / z = 622 [M + H]⁺</li><li>(4) 1- {2- [2- (morpholin-4-yl-carbonyl) -phenyl] -2-oxo-ethyl} -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.30 (silica gel, methylene chloride / methanol = 20: 1) Mass Spectrum (ESI⁺): m / z = 664 [M + H]⁺</li><li>(5) 1- (2- {2 - [(isopropylaminocarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8- [3- ( tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Implementation with Hünigbase in N, N-dimethylformamide) Mass Spectrum (ESI⁺): m / z = 650 [M + H]⁺</li><li>(6) 1- (2- {2 - [(ethylaminocarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8- [3- ( tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Implementation with Hünigbase in N, N-dimethylformamide) Mass Spectrum (ESI⁺): m / z = 636 [M + H]⁺</li><li>(7) 1- (2- {2- [2-Oxo-2- (pyrrolidin-1-yl) -ethoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (2-butyne) 1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Implementation with Hünigbase in N, N-dimethylformamide) Mass Spectrum (ESI⁺): m / z = 662 [M + H]⁺</li><li>(8) 1- (2- {2- [2- (morpholin-4-yl) -2-oxo-ethoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (2-butyne) 1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (Implementation with Hünigbase in N, N-dimethylformamide) Mass Spectrum (ESI⁺): m / z = 678 [M + H]⁺</li><li>(9) 1- (2- {2 - [(Methylaminocarbonyl) methylamino] -phenyl} -2-oxo-ethyl) -3-methyl-7 - ((E) -2-buten-1-yl) -8- [(R) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.40 (silica gel, cyclohexane / ethyl acetate / methanol = 5: 4: 1) Mass Spectrum (ESI⁺): m / z = 623 [M + H]⁺</li><li>(10) 1 - [(2-Amino-phenylaminocarbonyl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] xanthine R_fValue: 0.40 (silica gel, cyclohexane / ethyl acetate / methanol = 5: 4: 1) Mass Spectrum (ESI⁺): m / z = 565 [M + H]⁺</li></ol>

Example XXXIII

1-Chloromethyl-4-methyl-isoquinoline hydrochloride

0081prepared by treating (4-methyl-isoquinolin-1-yl) -methanol with thionyl chloride in methylene chloride. R_fValue: 0.76 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 95: 5: 0.1) Mass Spectrum (ESI⁺): m / z = 192, 194 [M + H]⁺

0082Analogously to Example XXXIII, the following compounds are obtained:<ol id="ol0022"><li>(1) 1-Chloromethyl-3,4-dimethylisoquinoline hydrochloride R_fValue: 0.65 (silica gel, petroleum ether / ethyl acetate = 2: 1) Mass Spectrum (ESI⁺): m / z = 206, 208 [M + H]⁺</li><li>(2) 5-Chloromethyl-8-methoxy-quinoline hydrochloride Mass Spectrum (ESI⁺): m / z = 208, 210 [M + H]⁺</li><li>(3) 8-Chloromethyl-5-methoxy-quinoline hydrochloride Mass spectrum (EI): m / z = 207, 209 [M]⁺</li><li>(4) 2-Chloromethyl-3-methylimidazo [1,2-a] pyridine hydrochloride R_fValue: 0.55 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 181, 183 [M + H]⁺</li><li>(5) 8-Chloromethyl-5-methoxy-isoquinoline hydrochloride Mass Spectrum (ESI⁺): m / z = 208, 210 [M + H]⁺</li><li>(6) 1-Chloromethyl-3,4-dimethyl-6,7-dihydro-5<i>H</i>- [2] pyrindin hydrochloride R_fValue: 0.50 (alumina, petroleum ether / ethyl acetate = 10: 1) Mass Spectrum (ESI⁺): m / z = 196, 198 [M + H]⁺</li><li>(7) 1-Chloromethyl-3,4-dimethyl-5,6,7,8-tetrahydro-isoquinoline hydrochloride R_fValue: 0.50 (alumina, petroleum ether / ethyl acetate = 10: 1) Mass Spectrum (ESI⁺): m / z = 210, 212 [M + H]⁺</li><li>(8) 6-Chloromethyl-2,3,8-trimethyl-quinoxaline hydrochloride Mass Spectrum (ESI⁺): m / z = 221, 223 [M + H]⁺</li><li>(9) 6-Chloromethyl-8-methylquinoxaline hydrochloride Mass Spectrum (ESI⁺): m / z = 193.195 [M + H]⁺</li><li>(10) 6-Chloromethyl-1,2,3,4-tetrahydrophenanthridine hydrochloride R_fValue: 0.50 (silica gel, petroleum ether / ethyl acetate = 5: 1) Mass Spectrum (ESI⁺): m / z = 232, 234 [M + H]⁺</li></ol>

Example XXXIV

1 - [(4-oxo-3,4-dihydro-quinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert.-butyloxycarbonylamino) piperidin-1-yl] -xanthine

0083To a solution of 428 mg of 1-cyanomethyl-3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine in 3 ml of methanol 0.5 ml of a 1 M solution of sodium methoxide in methanol are added dropwise at room temperature. After about 20 minutes, the resulting thick suspension is gently heated in a water bath and diluted with 2 ml of methanol. As soon as the conversion to the iminoester by thin layer chromatography is complete, the reaction mixture is neutralized with 0.5 ml of 1 M glacial acetic acid solution in methanol and treated with a solution of 130 mg of anthranilic acid in 2 ml of methanol. Gentle heating produces a clear solution which is stirred for 2.5 hours at room temperature. Subsequently, the reaction mixture is heated for about 3.5 hours under gentle reflux. After standing overnight at room temperature, the methanol is distilled off and the residue is stirred with cold water, filtered off with suction and dried. The crude product is suspended in 5 ml of methanol, heated slightly and filtered with suction after cooling, washed with methanol and dried in a desiccator. Yield: 302 mg (56% of theory) R_fValue: 0.55 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 575 [M + H]⁺

0084Analogously to Example XXXV, the following compounds are obtained:<ol id="ol0023" compact="compact"><li>(1) (4-Difluoromethoxy-naphthalen-1-yl) -methanol R_fValue: 0.33 (silica gel, cyclohexane / ethyl acetate = 6: 4) Mass Spectrum (ESI^-): m / z = 223 [MH]^-</li></ol>

Example XXXV

(4-Dimethylamino-naphthalen-1-yl) -methanol

0085prepared by reduction of 4-dimethylamino-naphthalene-1-carbaldehyde with sodium borohydride in aqueous tetrahydrofuran. R_fValue: 0.67 (silica gel, cyclohexane / ethyl acetate = 1: 1)

Example XXXVI

2-bromo-1- (2,3-dihyrdro-benzo [1,4] dioxin-5-yl) -ethanone

0086prepared by bromination of 1- (2,3-dihydro-benzo [1,4] dioxin-5-yl) -ethanone in methylene chloride with gentle ice bath cooling. The by-produced dibromo compound is separated by column chromatography. Mass Spectrum (ESI⁺): m / z = 257, 259 [M + H]⁺R_fValue: 0.92 (silica gel, methylene chloride)

0087The following compounds are obtained analogously to Example XXXVI:<ol id="ol0024" compact="compact"><li>(1) 7- (2-Bromo-acetyl) -3-methyl-3<i>H</i>-benzooxazol-2-one (Bromination is carried out in dioxane at 40 ° C, the product is contaminated with about 20% dibromo compound) R_fValue: 0.44 (silica gel, petroleum ether / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 270, 272 [M + H]⁺</li><li>(2) 1-Benzo [1,3] dioxol-4-yl-2-bromo-ethanone Mass Spectrum (ESI⁺): m / z = 243, 245 [M + H]⁺R_fValue: 0.94 (silica gel, methylene chloride)</li><li>(3) 2- [2- (2-Bromo-acetyl) -phenoxy] -<i>N</i>ethyl-acetamide (Bromination is carried out with copper (II) bromide in dioxane) Mass Spectrum (ESI⁺): m / z = 300, 302 [M + H]⁺</li><li>(4) 4- (2-Bromo-acetyl) -3-methyl-3<i>H</i>-benzooxazol-2-one R_fValue: 0.67 (silica gel, methylene chloride / methanol = 99: 1) Mass Spectrum (ESI⁺): m / z = 270, 272 [M + H]⁺</li><li>(5) 2- [2- (2-bromo-acetyl) -phenoxy] -<i>N</i>-methyl-acetamide Mass Spectrum (ESI⁺): m / z = 386, 388 [M + H]⁺</li><li>(6) 7- (2-Bromo-acetyl) -3 - [(2-trimethylsilanylethoxy) methyl] -3<i>H</i>-benzooxazol-2-one R_fValue: 0.84 (silica gel, methylene chloride / methanol = 99: 1) Mass Spectrum (ESI⁺): m / z = 384, 386 [M + H]⁺</li><li>(7) 4- (2-Bromo-acetyl) -1,3-dimethyl-1,3-dihydro-benzoimidazol-2-one R_fValue: 0.38 (silica gel, ethyl acetate / petroleum ether = 1: 1) Mass Spectrum (ESI⁺): m / z = 283, 285 [M + H]⁺</li><li>(8) 4- (2-Bromo-acetyl) -3 - [(2-trimethylsilanylethoxy) methyl] -3<i>H</i>-benzooxazol-2-one R_fValue: 0.82 (silica gel, methylene chloride / methanol = 99: 1)</li><li>(9) 4- (2-Bromo-acetyl) -1-ethoxycarbonyl-3-methyl-1,3-dihydro-benzoimidazol-2-one R_fValue: 0.39 (silica gel, petroleum ether / ethyl acetate = 2: 1) Mass Spectrum (ESI⁺): m / z = 341, 343 [M + H]⁺</li><li>(10) 2-bromo-1- (2,2-difluoro-benzo [1,3] dioxol-4-yl) -ethanone Mass Spectrum (ESI^-): m / z = 277, 279 [MH]^-</li></ol>

Example XXXVII

(2,3-dihydro-benzo [1,4] dioxin-5-yl) -ethanone

0088prepared by reacting 1- (2,3-dihydroxyphenyl) ethanone with 1,2-dibromoethane in the presence of potassium carbonate in N, N-dimethylformamide at 100 ° C. R_fValue: 0.43 (silica gel, ethyl acetate / petroleum ether = 1: 4) Mass Spectrum (ESI⁺): m / z = 179 [M + H]⁺

Example XXXVIII

1 - [(3-methyl-4-oxo-3,4-dihydro-quinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert .-butyloxycarbonylamino) -piperidin-1-yl] -xanthine

0089prepared by reacting 1 - [(4-oxo-3,4-dihydroquinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert .-Butyloxycarbonylamino) -piperidin-1-yl] -xanthine with methyl iodide in the presence of potassium carbonate in N, N-dimethylformamide at room temperature. R_fValue: 0.50 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 589 [M + H]⁺

0090The following compounds are obtained analogously to Example XXXVIII:<ol id="ol0025"><li>(1) 7-acetyl-3-methyl-3<i>H</i>-benzooxazol-2-one (The methylation is carried out in the presence of sodium carbonate in methanol) R_fValue: 0.46 (silica gel, petroleum ether / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 192 [M + H]⁺</li><li>(2) 4-acetyl-3-methyl-3<i>H</i>-benzooxazol-2-one (The methylation is carried out in the presence of sodium carbonate in methanol under reflux) R_fValue: 0.67 (silica gel, methylene chloride / methanol = 99: 1) Mass Spectrum (ESI⁺): m / z = 192 [M + H]⁺</li><li>(3) 4-Acetyl-1,3-dimethyl-1,3-dihydro-benzoimidazol-2-one (Carrying out in the presence of potassium tert-butoxide) R_fValue: 0.40 (silica gel, ethyl acetate / petroleum ether = 2: 1) Mass Spectrum (ESI⁺): m / z = 205 [M + H]⁺</li><li>(4) 4-Acetyl-1-ethoxycarbonyl-3-methyl-1,3-dihydro-benzoimidazol-2-one R_fValue: 0.23 (silica gel, petroleum ether / ethyl acetate = 2: 1) Mass Spectrum (ESI⁺): m / z = 263 [M + H]⁺</li><li>(5) 1 - [(1-methyl-1<i>H</i>-benzoimidazol-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine Mass Spectrum (ESI⁺): m / z = 561 [M + H]⁺</li><li>(6) 1 - {[1- (2-Cyanoethyl) -1H-benzoimidazol-2-yl] methyl} -3-methyl-7- (2-butyn-1-yl) -8- [3- ( tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.50 (silica gel, cyclohexane / ethyl acetate / methanol = 5: 4: 1) Mass Spectrum (ESI⁺): m / z = 600 [M + H]⁺</li><li>(7) 1 - ({1 - [(Methylaminocarbonyl) methyl] -1H-benzoimidazol-2-yl} methyl) -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert .-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.45 (silica gel, cyclohexane / ethyl acetate / methanol = 5: 4: 1) Mass Spectrum (ESI⁺): m / z = 618 [M + H]⁺</li><li>(8) 1 - [(1-Benzyl-1H-benzoimidazol-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) - piperidin-1-yl] -xanthine R_fValue: 0.50 (silica gel, cyclohexane / ethyl acetate / methanol = 5: 4: 1) Mass Spectrum (ESI⁺): m / z = 637 [M + H]⁺</li></ol>

Example XXXIX

1- [2- (2-cyanomethylamino-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino ) piperidin-1-yl] -xanthine

0091prepared by reacting 1- [2- (2-amino-phenyl) -2-oxo-ethyl] -3-methyl-7- (3-methyl-2-buten-1-yl) -8- tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine with paraformaldehyde and potassium cyanide in the presence of zinc chloride in glacial acetic acid at 40 ° C. R_fValue: 0.45 (silica gel, cyclohexane / ethyl acetate = 3: 7) Mass Spectrum (ESI⁺): m / z = 605 [M + H]⁺

Example XL

1- [2- (2-Amino-phenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>S</i>) - 3- (tert -butyloxycarbonylamino) -piperidin-1-yl] -xanthine

0092prepared by reduction of 1- [2- (2-nitrophenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>S</i>) -3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine with sodium dithionite in a mixture of methyl glycol and water (2: 1) at 100 ° C. R_fValue: 0.34 (silica gel, methylene chloride / methanol = 95: 5)

0093The following compounds are obtained analogously to Example XL:<ol id="ol0026" compact="compact"><li>(1) 1- [2- (2-Amino-phenyl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8 - [(<i>R</i>) -3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine R_fValue: 0.50 (silica gel, cyclohexane / ethyl acetate = 4: 6)</li></ol>

Example XLI

2-chloromethyl-4-methyl-quinazoline

0094prepared by treating 2.95 g of 2-chloromethyl-4-methyl-quinazoline-3-oxide with 6 ml of phosphorus trichloride in 150 ml of chloroform under reflux. Yield: 1.75 g (57% of theory) R_fValue: 0.81 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 193, 195 [M + H]⁺

Example XLII

2-chloromethyl-4-dimethylamino-quinazoline

0095To 500 mg of 4-chloro-2-chloromethyl-quinazoline in 5 ml of tetrahydrofuran is added dropwise with ice bath cooling a freshly prepared solution of 202 mg of dimethylamine in 3.2 ml of tetrahydrofuran. The reaction mixture is then stirred for 3.5 hours under ice-bath cooling and a further 30 minutes at room temperature. Then the solvent is gently distilled off on a rotary evaporator and the residue taken up in methylene chloride. The solution is washed with saturated sodium bicarbonate solution and with water, dried over magnesium sulfate and concentrated. The solid residue is stirred with a little tert-butyl methyl ether, filtered off, washed with petroleum ether and dried in vacuo. Yield: 323 mg (62% of theory) R_fValue: 0.60 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 222, 224 [M + H]⁺

0096The following compounds are obtained analogously to Example XLII:<ol id="ol0027"><li>(1) 2-Chloromethyl-4- (morpholin-4-yl) quinazoline R_fValue: 0.50 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 264, 266 [M + H]⁺</li><li>(2) 2-Chloromethyl-4- (piperidin-1-yl) quinazoline R_fValue: 0.70 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 262, 264 [M + H]⁺</li><li>(3) 4- [4- (tert-Butyloxycarbonyl) -piperazin-1-yl] -2-chloromethyl-quinazoline R_fValue: 0.57 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 363, 365 [M + H]⁺</li><li>(4) 2-Chloromethyl-4- (pyrrolidin-1-yl) quinazoline R_fValue: 0.50 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 248, 250 [M + H]⁺</li><li>(5) 2-Chloromethyl-4-ethoxy-quinazoline (The reaction is carried out with sodium ethanolate in ethanol at room temperature.) R_fValue: 0.50 (silica gel, cyclohexane / ethyl acetate = 3: 1) Mass Spectrum (ESI⁺): m / z = 223, 225 [M + H]⁺</li><li>(6) 2-Chloromethyl-4-isopropyloxy-quinazoline (The reaction is carried out with sodium isopropoxide in isopropanol at room temperature.) R_fValue: 0.70 (silica gel, cyclohexane / ethyl acetate = 3: 1) Mass Spectrum (ESI⁺): m / z = 237, 239 [M + H]⁺</li><li>(7) 2-Chloromethyl-4-phenyloxy-quinazoline (The reaction is carried out with sodium hydride and phenol in tetrahydrofuran at room temperature.) R_fValue: 0.65 (silica gel, cyclohexane / ethyl acetate = 3: 1) Mass Spectrum (ESI⁺): m / z = 271, 273 [M + H]⁺</li></ol>

Example XLIII

1- (2- {2 - [(ethoxycarbonyl) methylamino] -phenyl} -2-oxo-ethyl) -3-methyl-7 - ((E) -2-buten-1-yl) -8- [3- (tert-butyloxvcarbonylamino) piperidin-1-yl] -xanthine

0097To 531 mg of 1- [2- (2-amino-phenyl) -2-oxo-ethyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8- [3- (tert .-Butyloxycarbonylamino) -piperidin-1-yl] -xanthin and 10 mg of methyltrioxorhenium in 4.5 ml of toluene is added dropwise at room temperature under argon atmosphere, a solution of 110 .mu.L Diazoessigsäureethylester in 0.5 ml of toluene. The reaction mixture is stirred for 15 hours at room temperature. Then again about 5 mg Methyltrioxorhenium and 20 .mu.L Diazoessigsäureethylester are added and the reaction mixture is heated to 50 ° C for two hours. After cooling to room temperature, another 5 mg of methyltrioxorhenium and 20 .mu.l of diazoacetic acid ethyl ester are added. After a further 16 hours at room temperature, the reaction mixture with 5 ml of conc. aqueous ammonia, shaken and placed on an Extrelut packing. After 15 min, rinsed with 200 ml of methylene chloride. The methylene chloride solution is concentrated and chromatographed on a silica gel column with cyclohexane / ethyl acetate / isopropanol (8: 2: 0 to 8: 1: 1) as the eluent. Yield: 220 mg (36% of theory) R_fValue: 0.40 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 638 [M + H]⁺

Example XLIV

1 - -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl [(2-cyano-benzofuran-3-yl) methyl] ] xanthine

0098A mixture of 215 mg of 1- {2- [2-cyanomethoxyphenyl] -2-oxo-ethyl} -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert. butyloxycarbonylamino) -piperidin-1-yl] -xanthine and 244 mg of cesium carbonate in 4 ml of N, N-dimethylformamide is stirred at 50 ° C. for two hours, then at 70 ° C. for a further three hours. For working up, the reaction mixture is mixed with water and the resulting precipitate is filtered off with suction and dried. Yield: 130 mg (62% of theory) Mass Spectrum (ESI⁺): m / z = 572 [M + H]⁺

Example XLV

1- [2- (3-methyl-2-oxo-2,3-dihydro-1<i>H</i>-benzoimidazol-4-yl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert.-butyrloxycarbonylamino) piperidin-1-yl] - xanthine

0099prepared by treating 1- [2- (1-ethoxycarbonyl-3-methyl-2-oxo-2,3-dihydro-1<i>H</i>-benzoimidazol-4-yl) -2-oxo-ethyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] - xanthine with 1 N sodium hydroxide solution in methanol at room temperature. R_fValue: 0.36 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 605 [M + H]⁺

Example XLVI

4-acetyl-1-ethoxycarbonyl-1,3-dihydro-benzoimidazol-2-one

0100To 1.50 g of 1- (2,3-diamino-phenyl) -ethanone in 75 ml of methylene chloride are added 5.29 g of diethyl dicarbonate and 611 mg of dimethylaminopyridine. The reaction mixture is stirred for three hours at room temperature, then another 100 mg of dimethylaminopyridine and 1 ml of diethyl dicarbonate are added and the mixture is stirred at room temperature for a further 20 hours. For workup, the reaction mixture is diluted with methylene chloride, washed with 2N citric acid solution and saturated sodium bicarbonate solution and saturated sodium chloride solution, dried over magnesium sulfate and concentrated. The residue is chromatographed on a silica gel column with petroleum ether / ethyl acetate (3: 1 to 1: 2) as the eluent. The desired product is stirred with a little tert-butyl methyl ether, filtered off with suction, washed with a little ethyl acetate and tert. Yield: 900 mg (36% of theory) R_fValue: 0.15 (silica gel, petroleum ether / ethyl acetate = 2: 1) Mass Spectrum (ESI⁺): m / z = 249 [M + H]⁺

Example XLVII

1 - [(4-Amino-quinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl ] xanthine

0101To a mixture of 17 mg of potassium tert-butoxide in 10 ml of methanol are added 501 mg of 1-cyanomethyl-3-methyl-7- (2-butyn-1-yl) -8- [3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine. After brief heating with stirring ensteht a clear solution and after about 20 minutes, the nitrile is largely converted by thin-layer chromatogram to the iminoester. Now 206 mg of 2-amino-benzamidine hydrochloride are added and the reaction mixture is heated under reflux for four hours. After cooling to room temperature, the resulting precipitate is filtered off with suction, washed with methanol and dried. Yield: 143 mg (23% of theory) R_fValue: 0.15 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 574 [M + H]⁺

Example XLVIII

1- (2-phenyl-2-oxo-ethyl) -3-methyl-7 - ((Z) -2-buten-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1 yl-xanthine

0102150 mg of 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] Exxanthin are hydrogenated in a mixture of 5 ml of tetrahydrofuran and 5 ml of methanol in the presence of 30 mg of 5% palladium on activated carbon (poisoned with quinoline) at room temperature until the calculated amount of hydrogen is taken up. Then a spatula tip of activated charcoal is added and sucked off. The filtrate is concentrated and the crude product is purified by chromatography on a silica gel column with cyclohexane / ethyl acetate (7: 3 to 4: 6). Yield: 120 mg (85% of theory) R_fValue: 0.40 (silica gel, cyclohexane / ethyl acetate = 4: 6) Mass Spectrum (ESI⁺): m / z = 537 [M + H]⁺

Example XLIX

8-hydroxymethyl-5-methoxy-quinoline

0103To a solution of 640 mg of 8-hydroxymethyl-quinolin-5-ol in N, N-dimethylformamide are added under ice bath cooling in portions 148 mg of sodium hydride (about 60% in mineral oil) and the reaction mixture is slowly warmed to room temperature. After the evolution of gas has ended, 230 .mu.l of methyl iodide are added dropwise while cooling with an ice bath, then the reaction mixture is stirred for a further 2 hours at room temperature. For workup, it is poured onto ice-water, saturated with sodium chloride and extracted with a mixture of diethyl ether and ethyl acetate. The combined extracts are washed with saturated sodium chloride solution, dried over magnesium sulfate and concentrated. The flask residue is triturated with petroleum ether and the supernatant is decanted off. Yield: 470 mg (68% of theory) R_fValue: 0.70 (silica gel, ethyl acetate) Mass Spectrum (ESI⁺): m / z = 190 [M + H]⁺

0104The following compounds are obtained analogously to Example XLIX:<ol id="ol0028" compact="compact"><li>(1) 8-hydroxymethyl-5-methoxy-isoquinoline R_fValue: 0.40 (silica gel, methylene chloride / methanol = 10: 1) Mass Spectrum (ESI⁺): m / z = 190 [M + H]⁺</li></ol>

Example L

8-hydroxymethyl-quinoline-5-ol

01053.40 g of quinolin-5-ol is concentrated under ice bath cooling with 8 ml. Hydrochloric acid and 8 ml of 37% formalin solution. Then, hydrogen chloride gas is passed through the reaction mixture for about two hours, with the temperature rising slowly. The reaction mixture is stirred overnight first under ice-bath cooling, then at room temperature and then concentrated in vacuo. The flask residue is taken up in water, covered with diethyl ether and adjusted to pH 10 with ice-bath cooling and vigorous stirring with dilute ammonia solution. After a further two hours of vigorous stirring at room temperature, the organic phase is separated off and the aqueous phase is extracted with diethyl ether. The combined organic phases are washed with water and saturated sodium chloride solution, dried over magnesium sulfate and concentrated. The flask residue is chromatographed on a silica gel column with methylene chloride / methanol (20: 1) as the eluent. Yield: 660 mg (16% of theory) Mass Spectrum (ESI⁺): m / z = 176 [M + H]⁺

0106Analogously to Example L, the following compounds are obtained:<ol id="ol0029" compact="compact"><li>(1) 8-hydroxymethylisoquinolin-5-ol R_fValue: 0.50 (silica gel, methylene chloride / methanol = 5: 1) Mass Spectrum (ESI⁺): m / z = 176 [M + H]⁺</li></ol>

Example LI

1 - [(2-Cyclopropyl-quinazolin-4-yl) methyl] -3-methyl-7 - [(1-cyclopenten-1-yl) methyl] -8- [3- (tert.-butyloxycarbonylamino) -piperidin 1-yl] -xanthine

0107A mixture of 250 mg of 1- (2- {2 - [(cyclopropylcarbonyl) amino] -phenyl} -2-oxo-ethyl) -3-methyl-7 - [(1-cyclopenten-1-yl) methyl] -8 - [3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine and 7.5 ml of ethanolic ammonia solution (6 M) is heated in a bomb at 150 ° C for seven hours. For workup, the reaction mixture is concentrated and chromatographed on a silica gel column with methylene chloride / methanol (100: 0 to 70:30) as the eluent. The contaminated product fraction is concentrated and purified again on a reversed phase HPLC column with water / acetonitrile / trifluoroacetic acid (65: 15: 0.08 to 0: 100: 0.1) as the eluent. The product fractions are concentrated, made alkaline with dilute sodium hydroxide solution and extracted with methylene chloride. The combined extracts are dried over magnesium sulfate and concentrated. Yield: 40 mg (14% of theory) R_fValue: 0.40 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 627 [M + H]⁺

Example LII

4- (2-bromo-acetyl) -1,3-bis - [(2-trimethylsilanyl-ethoxy) methyl] -1,3-dihydro-benzoimidazol-2-one

0108To 420 mg of 4-acetyl-1,3-bis - [(2-trimethylsilanyl-ethoxy) methyl] -1,3-dihydro-benzoimidazol-2-one in 5 ml of tetrahydrofuran under an argon atmosphere, 520 mg of 2-pyrrolidinone-hydrotribromid and Added 89 mg of 2-pyrrolidinone. The reaction mixture is heated under reflux for two hours and then sucked off while still warm. The filter cake is washed with tetrahydrofuran and the filtrate is concentrated, leaving 660 mg of a tan solid. This is stirred with a little methanol, filtered off, washed with a little methanol and dried. The crude product is reacted further without further purification. Yield: 430 mg (87% of theory) R_fValue: 0.23 (silica gel, petroleum ether / ethyl acetate = 9: 1) Mass spectrum (EI): m / z = 514, 516 [M]⁺

0109Analogously to Example LII, the following compounds are obtained:<ol id="ol0030"><li>(1) 7- (2-Bromo-acetyl) -1- (tert-butyloxycarbonyl) -1<i>H</i>indole R_fValue: 0.33 (silica gel, petroleum ether / ethyl acetate = 9: 1) Mass Spectrum (ESI⁺): m / z = 338, 340 [M + H]⁺</li><li>(2) 2-bromo-1- (3-isopropyloxy-phenyl) -ethanone (Carrying out with phenyltrimethylammonium tribromide in methylene chloride) R_fValue: 0.39 (silica gel, cyclohexane / ethyl acetate = 9: 1)</li><li>(3) 2-bromo-1- (3-difluoromethoxy-phenyl) -ethanone (Carrying out with phenyltrimethylammonium tribromide in methylene chloride) R_fValue: 0.24 (reversed phase DC precast plate (E. Merck), acetonitrile / water / trifluoroacetic acid = 50: 50: 1)</li></ol>

Example LIII

3-methyl-imidazo [1,2-a] pyridine-2-carboxylic acid methylester

0110A mixture of 1.91 g of 2-aminopyridine and 4.40 g of 3-bromo-2-oxo-butyric acid methyl ester in 40 ml of ethanol is refluxed for six hours and then allowed to stand for 2 days at room temperature. The solvent is distilled off on a rotary evaporator and the crude product purified by chromatography on a silica gel column with methylene chloride / methanol / metanolic ammonia solution (95: 4: 1 to 90: 9: 1) as the eluent. As a by-product, 560 mg of the ethyl ester are isolated. Yield: 2.09 g (54% of theory) R_fValue: 0.20 (silica gel, methylene chloride / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 191 [M + H]⁺

Example LIV

2-chloromethyl-4-isopropyl-quinazoline

0111A solution of 2.86 g of 1- (2-amino-phenyl) -2-methyl-propan-1-one and 1.33 ml of chloroacetonitrile in 14 ml of dioxane is passed with stirring at room temperature for about five hours, dry hydrogen chloride gas. Subsequently, the dioxane is largely distilled off in a water-jet vacuum. The honey-like residue is mixed with ice-water and the resulting suspension made alkaline with saturated potassium carbonate solution under ice-bath cooling. The precipitate is filtered off with suction, washed with water and dried. The crude product is purified by chromatography on a silica gel column with petroleum ether / methylene chloride (8: 2 to 0: 1) as eluent. Yield: 1.80 g (58% of theory) R_fValue: 0.30 (silica gel, methylene chloride / petroleum ether = 1: 1) Mass Spectrum (ESI⁺): m / z = 221, 223 [M + H]⁺

Example LV

1-chloromethyl-3-trifluoromethyl-3,4-dihydro-isoquinoline

0112To 4.00 g of polyphosphoric acid are 530 mg of N- (1-benzyl-2,2,2-trifluoro-ethyl) -2-chloro-acetamide (prepared by reacting 1-benzyl-2,2,2-trifluoro-ethylamine with chloroacetyl chloride in the presence of triethylamine) and 0.74 ml of phosphorus oxychloride. The viscous mixture is stirred for 1.5 hours at 130.degree. For workup, the cooled reaction mixture and treated with ice-water, stirred vigorously for ten minutes and filtered with suction. The filter cake is dissolved in ethyl acetate and the solution dried over magnesium sulfate and concentrated to leave a white solid. Yield: 415 mg (84% of theory) R_fValue: 0.55 (alumina, petroleum ether / ethyl acetate = 10: 1) Mass Spectrum (ESI⁺): m / z = 248, 250 [M + H]⁺

0113Analogously to Example LV, the following connection is obtained:<ol id="ol0031" compact="compact"><li>(1) 1-Methyl-3-trifluoromethyl-3,4-dihydro-isoquinoline (The starting material N- (1-benzyl-2,2,2-trifluoro-ethyl) -acetamide is obtained by reacting 1-benzyl-2,2,2-trifluoro-ethylamine with acetic anhydride.)</li></ol>

Example LVI

3-Brommetyl-1- (1-cyano-1-methyl-ethyl) -isoquinoline

0114A mixture of 375 mg of 1- (1-cyano-1-methyl-ethyl) -3-methylisoquinoline and 321 mg of N-bromosuccinimide in 5 ml carbon tetrachloride is treated with a spatula tip of 2,2-azobisisobutyronitrile and refluxed for about six hours heated. The cooled reaction mixture is filtered and concentrated. The piston residue is reacted further without further purification. R_fValue: 0.70 (silica gel, cyclohexane / ethyl acetate = 3: 1)

0115The following connections are obtained analogously to example LVI:<ol id="ol0032"><li>(1) 6-Bromomethyl-1 - [(2-trimethylsilanylethoxy) methyl] -1<i>H</i>quinoline-2-one</li><li>(2) 1-Bromomethyl-4-bromo-3-methoxy-isoquinoline</li><li>(3) 2-bromomethyl- [1,5] naphthyridine Mass spectrum (ESI +): m / z = 223, 225 [M + H] +</li><li>(4) 5-bromomethyl- [1,6] naphthyridine R_fValue: 0.48 (silica gel, ethyl acetate / methanol = 98: 2)</li><li>(5) 7-bromomethyl-5-phenylquinoxaline R_fValue: 0.85 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 299, 301 [M + H]⁺</li><li>(6) 4-bromomethyl- [1,5] naphthyridine R_fValue: 0.56 (silica gel, methylene chloride / ethyl acetate = 7: 3) Mass Spectrum (ESI⁺): m / z = 223, 225 [M + H]⁺</li><li>(7) 1-Bromomethyl-3-trifluoromethyl-isoquinoline Mass Spectrum (ESI⁺): m / z = 290, 292 [M + H]⁺</li><li>(8) 1-Bromomethyl-3-difluoromethyl-isoquinoline Mass Spectrum (ESI⁺): m / z = 272, 274 [M + H]⁺</li><li>(9) 1-Bromomethyl-4-chloro-3-methoxy-isoquinoline</li></ol>

Example LVII

1- (1-cyano-1-methyl-ethyl) -3-methyl-isoquinoline

0116To 1.60 g of 3-methyl-isoquinoline-N-oxide in 30 ml of toluene, 3.30 g of 2,2-Azoisobuttersäuredinitril be given. The reaction mixture is stirred for six hours at 85 ° C and then allowed to stand for two days at room temperature. For workup, the reaction mixture is extracted with 20% hydrochloric acid. The combined aqueous phases are diluted with methylene chloride, made alkaline with saturated potassium carbonate solution under ice bath cooling and extracted with methylene chloride. The combined methylene chloride extracts are dried over magnesium sulfate and concentrated. The residue is chromatographed on a silica gel column with cyclohexane as the eluent. Yield: 375 mg (18% of theory) Mass Spectrum (ESI⁺): m / z = 211 [M + H]⁺R_fValue: 0.75 (silica gel, cyclohexane / ethyl acetate = 3: 1)

Example LVIII

1- (2-cyanoimino-2-phenyl-ethyl) -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] -xanthine (e / Z mixture)

0117To 244 mg of 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl ] -xanthine in 7 ml of methylene chloride are added dropwise 0.48 ml of a 1 M solution of titanium tetrachloride in methylene chloride. Subsequently, 88 ul of 1,3-bis (trimethylsilyl) carbodiimide are added and the mixture is stirred for four hours at room temperature. For workup, the reaction mixture is diluted with methylene chloride and poured onto ice water. The organic phase is washed with 0.5 N citric acid, dried over magnesium sulfate and concentrated. The crude product is purified by chromatography on a silica gel column with methylene chloride / methanol (98: 2 to 95: 5) as the eluent. Yield: 206 mg (97% of theory) Mass Spectrum (ESI^-): m / z = 557 [MH]^-R_fValue: 0.16 (silica gel, cyclohexane / ethyl acetate = 1: 1)

Example LIX

1 - [(1H-benzoimidazol-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert.-butyloxycarbonylamino) -piperidin-1-yl] - xanthine

0118350 mg of 1 - [(2-amino-phenylaminocarbonyl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- [3- (tert -butyloxycarbonylamino) -piperidin-1-yl] - xanthine are refluxed in 3 ml of glacial acetic acid for two hours. The reaction mixture is then concentrated, the flask residue is treated with 5 ml of 1 M sodium hydroxide solution and washed with methylene chloride. Then the aqueous phase is acidified with 1 M hydrochloric acid and extracted with methylene chloride. The combined extracts are concentrated and chromatographed on a silica gel column with cyclohexane / ethyl acetate / methanol (6: 4: 0 to 5: 4: 1) as the eluent. Yield: 250 mg (74% of theory) Mass Spectrum (ESI⁺): m / z = 547 [M + H]⁺

Example LX

3,4-dimethyl-6,7-dihydro-5<i>H</i>- [2] pyrindin-1-carboxylic acid ethyl ester

0119Prepared by treatment of 1.16 g of 3,4-dimethyl-4α- (pyrrolidin-1-yl) -5,6,7,7a-tetrahydro-4a<i>H</i>- [2] pyrindin-1-carboxylic acid ethyl ester with 1.08 g of 70% 3-chloroperbenzoic acid in 50 ml of methylene chloride at room temperature. Yield: 850 mg (97% of theory) R_fValue: 0.30 (alumina, petroleum ether / ethyl acetate = 5: 1) Mass Spectrum (ESI⁺): m / z = 220 [M + H]⁺

0120The following compounds are obtained analogously to Example LX:<ol id="ol0033" compact="compact"><li>(1) Ethyl 3,4-dimethyl-5,6,7,8-tetrahydro-isoquinoline-1-carboxylate R_fValue: 0.35 (alumina, petroleum ether / ethyl acetate = 5: 1) Mass Spectrum (ESI⁺): m / z = 234 [M + H]⁺</li></ol>

Example LXI

3,4-dimethyl-4a- (pyrrolidin-1-yl) -5,6,7,7a-tetrahydro-4a<i>H</i>- [2] pyrindin-1-carboxylic acid ethyl ester

0121Prepared by reaction of 2.50 g of ethyl 5,6-dimethyl- [1,2,4] triazine-3-carboxylate with 2.74 g of 1- (cyclopenten-1-yl) -pyrrolidine in 25 ml of chloroform at room temperature. Yield: 3.00 g (75% of theory) R_fValue: 0.60 (alumina, petroleum ether / ethyl acetate = 5: 1) Mass Spectrum (ESI⁺): m / z = 291 [M + H]⁺

0122The following compounds are obtained analogously to Example LXI:<ol id="ol0034" compact="compact"><li>(1) Ethyl 3,4-dimethyl-4α-(pyrrolidin-1-yl) -4a, 5,6,7,8,8a-hexahydro-isoquinoline-1-carboxylate R_fValue: 0.60 (alumina, petroleum ether / ethyl acetate = 5: 1) Mass Spectrum (ESI⁺): m / z = 305 [M + H]⁺</li></ol>

Example LXII

2,3,8-trimethyl-quinoxaline-6-carboxylic acid methylester

0123Prepared by reacting 1.60 g of methyl 3,4-diamino-5-methylbenzoate with 0.86 ml of diacetyl in a mixture of water and ethanol under reflux. Yield: 1.53 g (80% of theory) R_fValue: 0.63 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 231 [M + H]⁺

0124Analogously to Example LXII, the following compounds are obtained:<ol id="ol0035"><li>(1) Methyl 8-methylquinoxaline-6-carboxylate (Reaction with glyoxal in water.) R_fValue: 0.55 (silica gel, cyclohexane / ethyl acetate = 1: 1) Mass Spectrum (ESI⁺): m / z = 203 [M + H]⁺</li><li>(2) 5-bromo-7-methylquinoxaline (Reaction is carried out with glyoxal in a water / ethanol mixture.) R_fValue: 0.75 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 223, 225 [M + H]⁺</li></ol>

Example LXIII

3,4-diamino-5-methyl-benzoic acid methylester

0125Prepared by reduction of 3-nitro-4-amino-5-methyl-benzoic acid methyl ester at a hydrogen partial pressure of 50 psi in the presence of Raney nickel in methanol at room temperature. R_fValue: 0.40 (silica gel, tert-butyl methyl ether)

Example LXIV

3-nitro-4-amino-5-methyl-benzoic acid methylester

0126Prepared by treating 3-nitro-4-acetylamino-5-methylbenzoic acid with hydrogen chloride gas in methanol at room temperature followed by refluxing. Mass Spectrum (ESI⁺): m / z = 211 [M + H]⁺R_fValue: 0.75 (silica gel, tert-butyl methyl ether / acetic acid = 99: 1)

Example LXV

1- (2-phenyl-2-oxo-ethyl) -3-metthyl-7 - ((E) -1-buten-1-yl) -8-bromo-xanthine

0127To 290 mg of 1- (2-phenyl-2-oxo-ethyl) -3-methyl-7- (1-phenylsulfanyl-butyl) -8-bromxanthine in 6 ml of hexafluoroisopropanol are added 0.13 ml of 35% hydrogen peroxide solution. The reaction mixture is stirred for one hour at room temperature, diluted with methylene chloride and washed with sodium thiosulfate solution. The organic phase is dried over magnesium sulfate and concentrated. The flask residue is taken up in 6 ml of toluene and refluxed for eight hours. The toluene is then distilled off in vacuo and the crude product is purified on a silica gel column with methylene chloride / methanol (100: 0 to 95: 5) as the eluent. Yield: 104 mg (45% of theory) R_fValue: 0.61 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 417, 419 [M + H]⁺

0128Analogously to example LXV, the following compounds are obtained:<ol id="ol0036" compact="compact"><li>(1) 3-Methyl-7- (3-methyl-1-buten-1-yl) -8-bromo-xanthine R_fValue: 0.24 (silica gel, methylene chloride / methanol = 95: 5) Mass Spectrum (ESI⁺): m / z = 313, 315 [M + H]⁺</li></ol>

Example LXVI

1-methanesulfonyloxymethyl-4-difluoromethoxy-naphthalen

0129Prepared by reaction of (4-difluoromethoxy-naphthalen-1-yl) -methanol with methanesulfonyl chloride in methylene chloride in the presence of triethylamine.

0130The following compounds are obtained analogously to Example LXVI:<ol id="ol0037"><li>(1) (E) -1-Methanesulfonyloxy-3- (2-nitro-phenyl) -2-propene</li><li>(2) (E) -1-Methanesulfonyloxy-3-pentafluorophenyl-2-propene</li><li>(3) (E) -1-Methanesulfonyloxy-3- (2-trifluoromethylphenyl) -2-propene</li><li>(4) (E) -1-Methanesulfonyloxy-3- (3-trifluoromethylphenyl) -2-propene</li><li>(5) (E) -1-Methanesulfonyloxy-3- (4-trifluoromethylphenyl) -2-propene</li></ol>

Example LXVII

7-methyl-5-phenyl-quinoxaline

0131A mixture of 400 mg of 5-bromo-7-methylquinoxaline, 244 mg of phenylboronic acid and 100 mg of tetrakis (triphenylphosphine) palladium in 12 ml of dioxane, 4 ml of methanol and 3.6 ml of 1M aqueous sodium carbonate solution is refluxed under an argon atmosphere for three hours , The reaction mixture is then concentrated and the residue is partitioned between ethyl acetate and water. The ethyl acetate phase is separated, dried over magnesium sulfate and concentrated. The crude product is purified by chromatography on a silica gel column with cyclohexane / ethyl acetate (85:15 to 70:30) as the eluent. Yield: 390 mg (66% of theory) R_fValue: 0.36 (silica gel, petroleum ether / ethyl acetate = 5: 1) Mass Spectrum (ESI⁺): m / z = 221 [M + H]⁺

Example LXVIII

1-methyl-3-trifluoromethyl-isoquinoline

0132Prepared by treating 905 mg of 1-chloromethyl-3-trifluoromethyl-3,4-dihydro-isoquinoline with 420 mg of potassium tert-butoxide in 10 ml of tetrahydrofuran at room temperature. Yield: 755 mg (98% of theory) Mass Spectrum (ESI⁺): m / z = 212 [M + H]⁺

0133The following compounds are obtained analogously to Example LXVIII:<ol id="ol0038" compact="compact"><li>(1) 1-Methyl-3-difluoromethyl-isoquinoline (Prepared from 1-methyl-3-trifluoromethyl-3,4-dihydro-isoquinoline) Mass Spectrum (ESI⁺): m / z = 194 [M + H]⁺</li></ol>

Example LXIX

4-chloro-3-methoxy-1-methyl-isoquinoline

0134Prepared by treating 3-methoxy-1-methylisoquinoline with sulfuryl chloride in methylene chloride. R_fValue: 0.30 (silica gel, cyclohexane) Mass Spectrum (ESI⁺): m / z = 208, 210 [M + H]⁺

Example LXX

3-cyclopropyl-8-bromo xanthine

0135Prepared by reaction of 3-cyclopropyl-xanthine with bromine in the presence of potassium carbonate in acetonitrile at 60 ° C. R_fValue: 0.65 (reversed phase DC precast plate (E. Merck), acetonitrile / water / trifluoroacetic acid = 50: 50: 1) Mass Spectrum (ESI⁺): m / z = 271, 273 [M + H]⁺

Example LXXI

1,2,3,4-tetrahydro-phenanthridin-6-yl-carboxylic acid ethyl ester

0136Analogous to that of <nplcit id="ncit0005" npl-type="s"><text>Gonsalves et al. described methods (Tetrahedron 1992, 48, 6821</text></nplcit>) is a solution of 3.90 g of ethyl 5,6,7,8-tetrahydro-benzo [1,2,4] triazine-3-carboxylate (<nplcit id="ncit0006" npl-type="s"><text>Sagi et al., Heterocycles 1989, 29, 2253</text></nplcit>) in 20 ml of dioxane to reflux. Then, with the help of two dropping funnels, 8.22 g of anthranilic acid and 7.02 g of isoamyl nitrite, each dissolved in 20 ml of dioxane, are added dropwise within 25 minutes. The reaction mixture is heated for a further 30 minutes under reflux. For workup, the cooled deep brown reaction solution is diluted with 150 ml of diethyl ether, washed with 100 ml of 2 N sodium hydroxide solution and with water, dried over magnesium sulfate and concentrated. The brown, oily flask residue is chromatographed on a silica gel column with ethyl acetate / petroleum ether (20:80 to 50:50) as the eluent. The product obtained is still somewhat contaminated, but is reacted further without further purification. Yield: 380 mg (8% of theory) R_fValue: 0.55 (silica gel, petroleum ether / ethyl acetate = 2: 1) Mass Spectrum (ESI⁺): m / z = 256 [M + H]⁺

Preparation of the end compounds:

Reference Example 2

1- (2- {2 - [(ethoxycarbonyl) methoxy] -phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) -8- (3- amino-piperidin-1-yl) -xanthine

0137A solution of 209 mg of 1- (2- {2 - [(ethoxycarbonyl) methoxy] phenyl} -2-oxo-ethyl) -3-methyl-7- (3-methyl-2-buten-1-yl) - 8- [3- (tert-butyloxycarbonylamino) -piperidin-1-yl] -xanthine in 4 ml of methylene chloride is treated with 1 ml of trifluoroacetic acid and stirred for half an hour at room temperature. For workup, the reaction mixture is diluted with methylene chloride and washed with saturated potassium carbonate solution. The organic phase is dried, concentrated and chromatographed on a silica gel column with methylene chloride / methanol (1: 0 to 4: 1) as the eluent. Yield: 153 mg (87% of theory) Mass Spectrum (ESI⁺): m / z = 553 [M + H]⁺

0138Analogously to Reference Example 2, the following compounds according to the invention are obtained:<ul id="ul0003" list-style="none"><li>(52) 1 - [(Quinolin-4-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- (3-amino-piperidin-1-yl) -xanthine (Carrying out with isopropanolic hydrochloric acid 5-6 M in methylene chloride) R_fValue: 0.52 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 458 [M + H]⁺</li><li>(55) 1 - [(Quinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- (3-amino-piperidin-1-yl) -xanthine (Carrying out with isopropanolic hydrochloric acid 5-6 M in methylene chloride) R_fValue: 0.20 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 95: 5: 0.1) Mass Spectrum (ESI⁺): m / z = 459 [M + H]⁺</li><li>(63) 1 - [(isoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- (3-amino-piperidin-1-yl) -xanthine (Carrying out with isopropanolic hydrochloric acid 5-6 M in methylene chloride) R_fValue: 0.42 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 458 [M + H]⁺</li><li>(64) 1 - [(4-Methoxynaphthalene-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- (3-aminopiperidin-1-yl) -xanthine (Carrying out with isopropanolic hydrochloric acid 5-6 M in methylene chloride) R_fValue: 0.14 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 95: 5: 0.1) Mass Spectrum (ESI⁺): m / z = 487 [M + H]⁺</li><li>(65) 1 - [(3-Methyl-isoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- (3-aminopiperidin-1-yl) -xanthine (Carrying out with isopropanolic hydrochloric acid 5-6 M in methylene chloride) Melting point: 155-158 ° C Mass Spectrum (ESI⁺): m / z = 472 [M + H]⁺</li><li>(69) 1 - [(4-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- (3-aminopiperidin-1-yl) xanthine (Carrying out with isopropanolic hydrochloric acid 5-6 M in methylene chloride) R_fValue: 0.46 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 472 [M + H]⁺</li><li>(72) 1 - [(Quinolin-6-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- (3-amino-piperidin-1-yl) -xanthine (Carrying out with isopropanolic hydrochloric acid 5-6 M in methylene chloride) R_fValue: 0.15 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 95: 5: 0.1) Mass Spectrum (ESI⁺): m / z = 458 [M + H]⁺</li><li>(74) 1 - [(isoquinolin-1-yl) methyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8- (3-amino-piperidin-1-yl) -xanthine (Procedure with isopropanolic hydrochloric acid 5-6 M in methylene chloride, the product still contains about 20% Z-isomer) R_fValue: 0.66 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 0.1) Mass Spectrum (ESI⁺): m / z = 460 [M + H]⁺</li><li>(80) 1 - [(quinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - ((<i>R</i>) -3-amino-piperidin-1-yl) -xanthine (Carrying out with isopropanolic hydrochloric acid 5-6 M in methylene chloride) Mass Spectrum (ESI⁺): m / z = 459 [M + H]⁺</li><li>(81) 1 - [(quinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - ((<i>S</i>) -3-amino-piperidin-1-yl) -xanthine (Carrying out with isopropanolic hydrochloric acid 5-6 M in methylene chloride) Mass Spectrum (ESI⁺): m / z = 459 [M + H]⁺</li><li>(82) 1 - [(quinazolin-2-yl) methyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - ((<i>S</i>) -3-aminopiperidine-1-yl) -xanthine (Procedure with isopropanolic hydrochloric acid 5-6 M in methylene chloride, the product still contains about 20% Z-isomer) R_fValue: 0.12 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 95: 5: 0.1) Mass Spectrum (ESI⁺): m / z = 461 [M + H]⁺</li><li>(83) 1 - [(quinazolin-2-yl) methyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - ((<i>R</i>) -3-aminopiperidine-1-yl) -xanthine (Procedure with isopropanolic hydrochloric acid 5-6 M in methylene chloride, the product still contains about 15% Z-isomer) R_fValue: 0.12 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 95: 5: 0.1) Mass Spectrum (ESI⁺): m / z = 461 [M + H]⁺</li><li>(84) 1 - [(3-Methylisoquinolin-1-yl) methyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - ((<i>R</i>) -3-amino-piperidin-1-yl) -xanthine (Procedure with isopropanolic hydrochloric acid 5-6 M in methylene chloride, the product still contains about 17% Z-isomer) R_fValue: 0.54 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 474 [M + H]⁺</li><li>(85) 1 - [(3-Methylisoquinolin-1-yl) methyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - ((<i>S</i>) -3-amino-piperidin-1-yl) -xanthine (Procedure with isopropanolic hydrochloric acid 5-6 M in methylene chloride, the product still contains about 17% Z-isomer) R_fValue: 0.54 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 474 [M + H]⁺</li><li>(129) 1 - [(3-methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - ((<i>S</i>) -3-aminopiperidine-1-yl) -xanthine (Carrying out with isopropanolic hydrochloric acid 5-6 M in methylene chloride) Melting point: 155-156.5 ° C Mass Spectrum (ESI⁺): m / z = 472 [M + H]⁺</li><li>(130) 1 - [(3-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - ((R) -3-aminopiperidin-1-yl ) xanthine (Carrying out with isopropanolic hydrochloric acid 5-6 M in methylene chloride) R_fValue: 0.52 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 472 [M + H]⁺</li><li>(131) 1 - [(4-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - ((<i>S</i>) -3-aminopiperidine-1-yl) -xanthine (Carrying out with isopropanolic hydrochloric acid 5-6 M in methylene chloride) R_fValue: 0.46 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 472 [M + H]⁺</li><li>(132) 1 - [(4-Methylisoquinolin-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - ((<i>R</i>) -3-aminopiperidine-1-yl) -xanthine (Carrying out with isopropanolic hydrochloric acid 5-6 M in methylene chloride) R_fValue: 0.46 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 472 [M + H]⁺</li><li>(133) 1 - [(4-Methylisoquinolin-1-yl) methyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - ((<i>S</i>) -3-amino-piperidin-1-yl) -xanthine (Carrying out with isopropanolic hydrochloric acid 5-6 M in methylene chloride) R_fValue: 0.48 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 474 [M + H]⁺</li><li>(134) 1 - [(4-Methylisoquinolin-1-yl) methyl] -3-methyl-7 - ((E) -2-buten-1-yl) -8 - ((<i>R</i>) -3-amino-piperidin-1-yl) -xanthine (Carrying out with isopropanolic hydrochloric acid 5-6 M in methylene chloride) Melting point: 167.5-172 ° C Mass Spectrum (ESI⁺): m / z = 474 [M + H]⁺</li><li>(137) 1 - [(4-methoxynaphthalen-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - ((<i>S</i>) -3-aminopiperidine-1-yl) -xanthine (Carrying out with isopropanolic hydrochloric acid 5-6 M in methylene chloride) R_fValue: 0.52 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 487 [M + H]⁺</li><li>(138) 1 - [(4-methoxynaphthalene-1-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8 - ((<i>R</i>) -3-aminopiperidine-1-yl) -xanthine (Carrying out with isopropanolic hydrochloric acid 5-6 M in methylene chloride) R_fValue: 0.52 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 487 [M + H]⁺</li><li>(141) 1 - [(4-Methyl-quinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- (3- (3)<i>S</i>) Aminopiperidine-1-yl) -xanthine (Carrying out with isopropanolic hydrochloric acid 5-6 M in methylene chloride) R_fValue: 0.51 (silica gel, methylene chloride / methanol / concentrated aqueous ammonia = 90: 10: 1) Mass Spectrum (ESI⁺): m / z = 473 [M + H]⁺</li><li>(142) 1 - [(4-Methylquinazolin-2-yl) methyl] -3-methyl-7- (2-butyn-1-yl) -8- (3- (R) -aminopiperidin-1-yl ) xanthine (Carrying out with isopropanolic hydrochloric acid 5-6 M in methylene chloride) Melting point: 198-202 ° C Mass Spectrum (ESI⁺): m / z = 473 [M + H]⁺</li></ul>

Example 4

Dragées with 75 mg active substance

0139<tables id="tabl0002" num="0002"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="47mm" /><colspec colnum="2" colname="col2" colwidth="19mm" /><thead><row><entry namest="col1" nameend="col2" align="left" valign="top">1 Dragéekern contains:</entry></row></thead><tbody><row><entry>active substance</entry><entry align="right">75.0 mg</entry></row><row><entry>calcium phosphate</entry><entry align="right">93.0 mg</entry></row><row><entry>corn starch</entry><entry align="right">35.5 mg</entry></row><row><entry>polyvinylpyrrolidone</entry><entry align="right">10.0 mg</entry></row><row><entry>hydroxypropyl methylcellulose</entry><entry align="right">15.0 mg</entry></row><row><entry>magnesium stearate</entry><entry rowsep="1" align="right">1.5 mg</entry></row><row><entry /><entry align="right">230.0 mg</entry></row></tbody></tgroup></table></tables>

production:

0140The active substance is mixed with calcium phosphate, corn starch, polyvinylpyrrolidone, hydroxypropylmethylcellulose and half of the stated amount of magnesium stearate. On a tabletting machine compacts are produced with a diameter of about 13 mm, these are ground on a suitable machine through a sieve with a mesh size of 1.5 mm and mixed with the remaining amount of magnesium stearate. This granulate is pressed on a tabletting machine into tablets of the desired shape.<tables id="tabl0003" num="0003"><table frame="none"><tgroup cols="2"><colspec colnum="1" colname="col1" colwidth="24mm" /><colspec colnum="2" colname="col2" colwidth="25mm" /><tbody><row><entry colsep="0" rowsep="0">Weight of core:</entry><entry colsep="0" rowsep="0">230 mg</entry></row><row><entry colsep="0" rowsep="0">Stamp:</entry><entry colsep="0" rowsep="0">9 mm, arched</entry></row></tbody></tgroup></table></tables>

0141The thus prepared dragee cores are coated with a film consisting essentially of hydroxypropylmethylcellulose. The finished Filmdragées are shined with beeswax. Dragée weight: 245 mg.

Example 5

0142<u>Tablets with 100 mg active substance</u>

Composition:

1 tablet contains:

0143<tables id="tabl0004" num="0004"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="32mm" /><colspec colnum="2" colname="col2" colwidth="19mm" /><tbody><row><entry>active substance</entry><entry align="right">100.0 mg</entry></row><row><entry>lactose</entry><entry align="right">80.0 mg</entry></row><row><entry>corn starch</entry><entry align="right">34.0 mg</entry></row><row><entry>polyvinylpyrrolidone</entry><entry align="right">4.0 mg</entry></row><row><entry>magnesium stearate</entry><entry rowsep="1" align="right">2.0 mg</entry></row><row><entry /><entry align="right">220.0 mg</entry></row></tbody></tgroup></table></tables>

Production process:

0144Active ingredient, lactose and starch are mixed and uniformly moistened with an aqueous solution of polyvinylpyrrolidone. After screening of the moist mass (2.0 mm mesh size) and drying in a rack oven at 50 ° C is again sieved (1.5 mm mesh) and the lubricant mixed. The ready-to-use mixture is processed into tablets.<tables id="tabl0005" num="0005"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="30mm" /><colspec colnum="2" colname="col2" colwidth="92mm" /><tbody><row><entry>Tablet weight:</entry><entry>220 mg</entry></row><row><entry>Diameter:</entry><entry>10 mm, biplan with facet on both sides and one-sided part notch.</entry></row></tbody></tgroup></table></tables>

Example 6

0145<u>Tablets with 150 mg active substance</u>

Composition:

1 tablet contains:

0146<tables id="tabl0006" num="0006"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="39mm" /><colspec colnum="2" colname="col2" colwidth="19mm" /><tbody><row><entry>active substance</entry><entry align="right">150.0 mg</entry></row><row><entry>Milk sugar powder.</entry><entry align="right">89.0 mg</entry></row><row><entry>corn starch</entry><entry align="right">40.0 mg</entry></row><row><entry>Colloidal silicic acid</entry><entry align="right">10.0 mg</entry></row><row><entry>polyvinylpyrrolidone</entry><entry align="right">10.0 mg</entry></row><row><entry>magnesium stearate</entry><entry rowsep="1" align="right">1.0 mg</entry></row><row><entry /><entry align="right">300.0 mg</entry></row></tbody></tgroup></table></tables>

production:

0147The active substance mixed with milk sugar, corn starch and silicic acid is moistened with a 20% strength aqueous solution of polyvinylpyrrolidone and beaten through a sieve with a mesh size of 1.5 mm.

0148The granules dried at 45 ° C are again rubbed through the same sieve and mixed with the stated amount of magnesium stearate. Out of the mix

0149Pressed tablets.<tables id="tabl0007" num="0007"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="30mm" /><colspec colnum="2" colname="col2" colwidth="23mm" /><tbody><row><entry>Tablet weight:</entry><entry align="right">300 mg</entry></row><row><entry>Stamp:</entry><entry align="right">10 mm, flat</entry></row></tbody></tgroup></table></tables>

Example 7

Hard gelatine capsules with 150 mg active substance

1 capsule contains:

0150<tables id="tabl0008" num="0008"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="32mm" /><colspec colnum="2" colname="col2" colwidth="22mm" /><tbody><row><entry>active substance</entry><entry align="right">150.0 mg</entry></row><row><entry>Corn starch drink.</entry><entry align="right">about 180.0 mg</entry></row><row><entry>Milk sugar powder.</entry><entry align="right">about 87.0 mg</entry></row><row><entry>magnesium stearate</entry><entry rowsep="1" align="right">3.0 mg</entry></row><row><entry /><entry align="right">about 420.0 mg</entry></row></tbody></tgroup></table></tables>

production:

0151The active ingredient is mixed with the excipients, passed through a sieve of 0.75 mm mesh size and mixed homogeneously in a suitable device. The final mixture is filled into size 1 hard gelatin capsules. Capsule filling: approx. 320 mg Capsule shell: hard gelatin capsule size 1

Example 8

Suppositories with 150 mg active substance

1 suppository contains:

0152<tables id="tabl0009" num="0009"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="56mm" /><colspec colnum="2" colname="col2" colwidth="20mm" /><tbody><row><entry>active substance</entry><entry align="right">150.0 mg</entry></row><row><entry>Polyethylene glycol 1500</entry><entry align="right">550.0 mg</entry></row><row><entry>Polyethylene glycol 6000</entry><entry align="right">460.0 mg</entry></row><row><entry>polyoxyethylene</entry><entry rowsep="1" align="right">840.0 mg</entry></row><row><entry /><entry align="right">2000.0 mg</entry></row></tbody></tgroup></table></tables>

production:

0153After the suppository mass has melted, the active ingredient is distributed homogeneously therein and the melt is poured into pre-cooled molds.

Example 9

Suspension with 50 mg active substance

0154100 ml suspension contain:<tables id="tabl0010" num="0010"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="55mm" /><colspec colnum="2" colname="col2" colwidth="19mm" /><tbody><row><entry>active substance</entry><entry align="right">1.00 g</entry></row><row><entry>Carboxymethylcellulose-Na-salt</entry><entry align="right">0.10 g</entry></row><row><entry>p-hydroxybenzoate</entry><entry align="right">0.05 g</entry></row><row><entry>p-hydroxybenzoate</entry><entry align="right">0.01 g</entry></row><row><entry>cane sugar</entry><entry align="right">10.00 g</entry></row><row><entry>glycerin</entry><entry align="right">5.00 g</entry></row><row><entry>Sorbitol solution 70%</entry><entry align="right">20.00 g</entry></row><row><entry>Aroma</entry><entry align="right">0.30 g</entry></row><row><entry>Water dist.</entry><entry align="right">ad 100 ml</entry></row></tbody></tgroup></table></tables>

production:

0155Dest. Water is heated to 70 ° C. Herein, p-hydroxybenzoic acid methyl ester and propyl ester and glycerol and carboxymethyl cellulose sodium salt are dissolved with stirring. It is cooled to room temperature and added with stirring, the active ingredient and dispersed homogeneously. After addition and dissolution of the sugar, the sorbitol solution and the aroma, the suspension is evacuated to vent with stirring. 5 ml of suspension contain 50 mg of active ingredient.

Examples 10

Ampoules with 10 mg active substance

Composition:

0156<tables id="tabl0011" num="0011"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="34mm" /><colspec colnum="2" colname="col2" colwidth="17mm" /><tbody><row><entry>active substance</entry><entry align="right">10.0 mg</entry></row><row><entry>0.01 n hydrochloric acid sq</entry><entry align="right" /></row><row><entry>Aqua bidest</entry><entry align="right">ad 2.0 ml</entry></row></tbody></tgroup></table></tables>

production:

0157The active substance is dissolved in the required amount of 0.01 N HCl, isotonic with sodium chloride, sterile filtered and filled into 2 ml ampoules.

Example 11

Ampoules with 50 mg active substance

Composition:

0158<tables id="tabl0012" num="0012"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="34mm" /><colspec colnum="2" colname="col2" colwidth="19mm" /><tbody><row><entry>active substance</entry><entry align="right">50.0 mg</entry></row><row><entry>0.01 n hydrochloric acid sq</entry><entry align="right" /></row><row><entry>Aqua bidest</entry><entry align="right">ad 10.0 ml</entry></row></tbody></tgroup></table></tables>

production:

0159The active ingredient is dissolved in the required amount of 0.01 N HCl, isotonic with saline, sterile filtered and filled into 10 ml ampoules.