Fungicide and method of efficient component production

The invention relates to a fungicide. The present invention relates to a process for the preparation of active compounds. I.

The present invention relates to a fungicidal composition, characterized in that it contains at least one compound of the formula I as active ingredient.

<img file="CS249506B2_D0001.tif" />

in which

R 7 and R 8 are each independently C 1 -C 4 alkyl or halogen;

R y represents a hydrogen atom, a C 1 -C 4 alkyl group or a halogen atom, and

R 10 represents a C 1 -C 4 alkoxyalkyl group, an alkoxy and alkyl moiety, a 2-furyl group, a halogenated 2-furyl group, or a 2-tetrahydrofuryl group, together with an agriculturally acceptable carrier or diluent.

The alkyl group R, R, R and Rg preferably contains 1 to 3 carbon atoms. Thus, for example, it is methyl, ethyl or n-propyl or isopropyl.

Suitable halogen atoms for R7, R5 and R8 are fluorine, chlorine, bromine or iodine, preferably chlorine or atom, and especially chlorine.

A preferred halogenated 2-furyl group R 10 is a monohalogenated 2-furyl group, for example a 5-chloro-2-furyl group and a 5-bromo-2-furyl group.

A preferred halogenated 2-tetrahydrofuryl group as defined by the symbol Rio is monohatogenated 2-tetra^:a hydrofuryl group, in particular a monochlorinated or mono-brominated 2-tetrahyidrofuryl group, such as a 5-chloro-2-tetrahydrofuryl group.

A preferred alkoxyalkyl group having 1 to 4 carbon atoms in the alkoxy and alkyl moiety as defined by R 10 is an alkoxymethyl group having 1 to 3 carbon atoms in the moiety, especially a group of the formula CH 5 OCH 2 - and C 2 H 5 OCH 2 -.

Preferably R10 is C1 -C4 alkoxyalkyl, alkyl or alkoxy, 2-furyl or 5-halo-2-furyl.

Preferred fungicidal compositions comprising as active ingredient at least one compound of formula (I) wherein:

R 7 and R 8 are each independently methyl, chlorine or bromine,

R 9 represents a hydrogen atom, a chlorine atom, a bromine atom or a methyl group;

R 10 is methoxymethyl, ethoxymethyl or 2-furyl.

Particularly preferred is a fungicidal composition which contains as an active ingredient at least one compound of the formula I in which:

R 7 and R 8 represent a methyl group,

R 9 represents a hydrogen atom and

R10. represents a methyl group.

According to the present invention, compounds of formula (I) are prepared by intramolecularly condensing a compound of formula (II)

<img file="CS249506B2_D0002.tif" />

X ⁰O β.

⁴ мн-ооо-сн-он-гУ

- (II) in which

Y represents a halogen atom, and

R 2, R 8, R 9 and R 10 are as defined above.

In formula II, Y is preferably chlorine or bromine, especially chlorine.

The Iotramolocular condensation according to the invention can be carried out in a manner known per se. Thus, it can be carried out, for example, in a water-free environment, using an ether, such as dimethoxyethane, a hydrocarbon, such as toluene as the solvent, or using another solvent which is inert under the reaction conditions. Temperature is not critical to the reaction. Preferably, the reaction temperature is between about 0 and 100 ° C. Since the reaction proceeds exothermically, it is usually initiated at room temperature and allowed to rise gradually.

The reaction is generally carried out in the presence of an acid binding agent, such as sodium hydride, sodium amide or sodium alkoxide, for example metboxide. sodium.

Intramolecular condensation can also be carried out in an aqueous-organic biphasic system, in the presence of an inorganic base such as sodium hydroxide and optionally in the presence of a catalytic amount of a phase transfer catalyst. The organic phase may be any suitable inert, water-immiscible solvent, such as hydrocarbons or halogenated hydrocarbons, for example xylene, toluene, o-dichlorobenzene or dichloromethane. Suitable phase transfer catalysts are quaternary ammonium compounds, such as beinzyl trimethylamcinium bromide, and quaternary phosphonium compounds, such as benzyltriphonylphosphoric chloride or ether, such as 18-crown-6.

The compounds of formula (II) are novel. These compounds can be prepared by acylating compounds of formula III

<img file="CS249506B2_D0003.tif" />

0-Y (III) wherein

R 7, R 8, R 9 and Y are as defined above with a compound of formula IV

O

R 10 —C — Z (IV) wherein

R 10 is as defined above and

Z represents a halogen atom, especially a chlorine atom, or represents a group of the formula -OCOR 10 wherein R 10 is as defined above.

Suitable solvents for this acylation reaction are hydrocarbons such as toluene or halogenated hydrocarbons such as chlorobenzene. This reaction is generally carried out at a temperature of about 50 to 120 ° C, for example at 80 ° C.

Compounds of formula III may be prepared by reaction of compounds of formula V

<img file="CS249506B2_D0004.tif" />

in which

R 7, R a and R 9 are as defined above, with a compound of formula VI

O

II

X — С —О — CH2 — CH2 — Y (VI) wherein

Y is as defined above and

X is halogen, especially chlorine.

This reaction can be carried out at temperatures from about 0 ^CC up to about 10 ° C in water or in an organic solvent which is inert under the reaction conditions, usually in the presence of a base, for example an organic amine or sodium bicarbonate.

The starting materials and reagents used in the processes described above are either known per se or, if they are not known, can be prepared by methods similar to those described or known per se.

In particular, the compounds of formula (I) have useful fungicidal activity against phytopathogenic fungi, in particular against fungi of the order Oomycetes, as evidenced by their potent activity in the tests described below.

Test A

Phytophthora inf estans fungicidal activity test

Young potted potato plants (3-5 leaf stage) are sprayed with an aqueous spray suspension containing 0.003 percent (w / v) of a compound of formula I, for example 2-methoxy-N- (2,6-dimethylphenyl) -N- ( 2-oxo-3-oxazolidinyl) acetamide (formulated in accordance with the formulation of Example 1). Two hours later, the treated plants are inoculated with a spore suspension of Phytophthora infestans, and the plants are then transferred to an area of ​​100% relative humidity at 16 ° C for 16 hours. Disease control is assessed after 4-5 days by comparing the treated plants with untreated plants similarly inoculated. Using the above test compound, a substantial reduction in fungal attack is observed without any sign of phytotoxicity for the host plant.

Test В

Fungicidal action against grapevine (Plasmoipara viticola)

Young, tanked vine plants (3-6 leaf stage) are sprayed with an aqueous spray suspension containing 0.000 8% (w / v) of a compound of formula I, for example 2-methoxy-N- (2,6-dimethylphenyl) -N- (2-oxo-3-oxazolidinyl) acetamide (formulated in accordance with the formulation of Example 1). Two hours later, the treated plants were inoculated with a spore suspension of the Plasmopara viticola peronospora, and the plants were then transferred to an area with 100% relative humidity at room temperature.

1. Tests carried out in the greenhouse

Compound of Example No. Plasmopara vine lot around 15-22 ° C (varying over a 24-hour period) and having a day length of 16 hours. Disease control is evaluated 6 days after inoculation by comparing treated plants with similarly inoculated untreated plants. Using the test compound, a substantial reduction in fungal attack is observed without any phytotoxicity to the host plant.

The results of the tests are summarized in the following tables:

ЕС 90 (ppm)

Phytophthora potato tomato

<td> 1</td><td> 11</td><td> 19</td><td> 32</td>

<td> 5</td><td>24 to 56</td><td> 72</td><td> 91</td>

<td> 26</td><td> 5</td><td>23 to 30</td><td> 185</td>

<td> 34</td><td> 56</td><td> 51</td><td> &gt; 500</td>

<td> 48</td><td> 72</td><td> 30</td><td> 30</td>

<td colspan="2">2. Field tests</td>

<td>The compound of Example no.</td><td>15 g of active ingredient / 100 L of Phytophthora / potatoes% of fungus suppression</td>

<td> 1</td><td> 94</td>

<td> 26</td><td> 99</td>

<td>Metalaxyl^{1 * * * * 6}]</td><td> 97</td>

<td>Legend:</td><td></td>

¹N- (2,6-dimethylphenyl) -N- (1'-methoxycarbonylethyl) methoxyacotamide (cf. French Patent Specification 2,267,042).

3. Phytotoxicity (0.6% aqueous solution of active substance, test plants: grapevine plants, evaluation 7 days after application)

Compound% phytotoxicity of Example. C.

0

Metalaxyl 60

Test C

Curative fungicidal action against peronospora of grapevine (Plasmopara viticola)

Young potato vine plants (stage 3 to leaf) are infected in the same manner as described in Test B, but treated with a compound of formula I, for example 2-methoxy-N- (2,6'-dimethylphenyl) -N- (2-oxo-3-oxazolidinyl) acetamide (formulated in accordance with the formulation of Example 1) only 3 days after infection. The incubation conditions are the same as in the assay

B. The control of fungal infestation is evaluated in the same manner as in Test B. Using the test compound, a significant reduction in fungal infestation of the plant is achieved.

Test D

Fungicidal effect for combating vine perenospora (Plasmopara viticola)

The method of evaluating this type of effect is the same as described in Test C, except that treatment is performed only 6 days after inoculation when sporulation of the lower leaf surface is already apparent. The infestation reduction is evaluated 7 days after treatment with, for example, 0.012% 2-methoxy-N- (2,6-dimethylphenyl) -N- (2-oxo-3-oxazolidinyl) acetamide (formulated in accordance with the formulation of Example 1); found not to expand the already sporulated zone, while sporulation perfectly ceases.

Test E

Translocation in treated vine leaves

The cut off vine leaves are treated with an aqueous spray suspension containing 0.012 percent of a compound of formula I, for example 2-methoxy-N- (2,6-dimethylphenyl) -N- (2-oxo-3-oxazolidinyl) acetamide (formulated in accordance with the formulation) according to Example 1), wherein only the lower part of such sheets is treated. Two hours after treatment, the whole leaf is inoculated with a spore suspension of Plasmopara viticola peronospora, whereupon the leaves are inhibited in a 100% humidity environment under the conditions of Test B. Although only the lower part of the leaves was treated as above, is treated with the test compound

249596 a substantial reduction in infestation when only the upper half of the leaves are treated. Thus, this test demonstrates that 2-methoxy-N- (2,6-dimethylphenyl) -N- (oxo-3-oxazolidinyl) Jacetamide (formulated in accordance with the formulation of Example 1) disperses within the sheet both acropetally and basipetally ( browse both length and thickness.

Test F

Soil treatment

Pythium aphanidermatum bag rot is used in vivo. The chase is cultivated in a sterile mixture of sand and corn meal (97: 3 v / v) to which water is added at a ratio of 1: 4 (v / v); the culture lasts 4 days at 25 ° C. The sponge is then mixed into a semi-sterile mixture of peat and feather, which is then treated with a suspension containing the formulated active ingredient to achieve a concentration of 10 to 160 ppm (e.g. 10, 40 and 160 ppm) based on substrate volume. The substrate is transferred to 5 cm diameter mugs which are sewn with cucumber seeds.

⁷ The sieved pots are incubated at 24 ^CC and at a relative humidity of 60 to 70% in an incubation room for 7 days, then assessing the extent of infection by comparing the number of healthy emerging plants with untreated, similarly inoculated test cups. The compound of formula (I) used as a wettable powder provides complete protection against attack. .

Tests similar to test F give similar results with peas and sugar beets.

Any of the following compounds in the following examples have been found to have fungicidal properties that determine its utility as a fungicide.

A particularly pronounced fungicidal effect has been observed in the tests described above for compounds of formula I in which:

R 10 is -CH 2 OC 2 H 5,

R2 and R2 are methyl and

R 8 represents a hydrogen atom, longer for those compounds of the general formula I in which

R 0 represents a 2-furyl group,

R @ 1 and R @ 3 are methyl and R @ 4 is hydrogen, furthermore, for those compounds of formula (I) in which R @ 1 and R @ 2 are each hydrogen

R 10 is 5-bromo-2-furyl, R 2 and R a are methyl, and R 8 is hydrogen, longer for those compounds of formula I wherein:

R 8 is -CH 2 OCH 3,

R 2 and R 5 are chlorine and

R 8 represents a hydrogen atom, as well as for compounds of formula I in which

R 10 is -CH 2 OCH 3,

R 2 and R 5 are methyl and

Rg is bromine at position 3.

and in particular, a compound of the general formula in which

R1.0 represents a group —Ci10OCHp

R 2 and R 5 are methyl and R 8 is hydrogen.

Fungicidal compositions which contain a compound of formula I as an active ingredient are therefore suitable for combating phytopathogenic fungi, in particular Oomycetes, on plants, seeds or soil, wherein the plants, seeds or soil are treated with a fungicidally effective amount of a compound of formula I.

Oornycetes fungi for which the fungicidal compositions of the invention are particularly effective include fungi of the genus Phytophthora on plants such as potatoes, tomatoes, tobacco, citrus, cacao, rubber, apple, strawberry, vegetables and ornamental plants. These include, for example, potato late blight (Phytophthora infestans) on potatoes and tomatoes; peronospora (Plasrnoinra viticola), fungi of the genus Perenospora on plants such as tobacco, for example, peronospora (Psronospora tabacina); fungi of the genus Pseudoperonospora in plants such as hops and cucumber, such as pseudoperonospora hops (Pseudoperonospora humuli); Bremia fungi on plants such as lettuce, for example, mold (Brem · a lactuca) on a tomato; Pythium hcubs, which cause fungus infestation of young plants, ie, "support" and root rot of a large number of plants such as vegetables, diabetes, ornamental plants and butterfly plants, such as Pythium sphanidermatum on diabetes; fungi of the genus Sclerospora, in particular on sorghum and cereals, for example Sclerospora sorgh's on sorghum.

The amount of the composition to be used according to the invention varies depending on such factors as the type of fungi to be treated, the duration of the treatment and the method of treatment and the type of compound of formula I used in the composition.

In general, however, satisfactory results are obtained when applied at the site, for example when applied to a crop or soil, at a dose of 0.05 to 5 kg, preferably 0.1 to 3 kg, of compound of the formula I per ha, repeats. when a fungicidal composition according to the invention which contains an active compound of the formula I is used for seed dressing, sufficient results are obtained if a dose of 0.05 to 0.5 g of the compound of the formula I per 1 is preferably 0.1 to 0 3 g of the compound of the formula I per kg of seed.

The compounds of formula (I) are used as fungicidal compositions together with noses and diluents which are acceptable in agriculture. In addition to the compounds of the general seed, generally

The active ingredients may also contain other active ingredients, such as fungicides, in particular fungicides based on copper compounds, as well as Captan, Folpet,

Mancozeb or Mane-b.

The compositions of the invention may be used in either solid or liquid dosage forms, for example, wettable powder, emulsion concentrate, water dispersible suspension concentrate, dust, granulate, retarding dosage form using conventional carriers. and / or adjuvants. Such compositions can be prepared by methods known in the art.

The fungicidal compositions according to the invention can in particular be used in the form of water-dispersible concentrates or wettable powders which are applied by spraying. These compositions may contain surfactants such as wetting and dispersing agents such as formaldehyde condensation products with naphthalene sulfonate, alkylsulfonyl sulfonate, lignin sulfonate, alkyl sulfates derived from higher aliphatic hydrocarbons, ethoxylated alkylphenol and ethoxylated fatty alcohol.

In general, the fungicidal compositions according to the invention contain from 0.01 to 90% by weight of active compound, the active compound being optionally present together with other fungicidally active compounds.

The concentrates generally contain between 2 and 80% by weight, preferably between 5 and 70% by weight. The liquid dosage forms of the compositions according to the invention may contain from 0.01 to 20% by weight, preferably from 0.01 to 5% by weight, of the active ingredient.

The invention is further illustrated by the following examples in which parts and percentages are by weight and percentages. However, these examples do not limit the scope of the invention in any way.

Example of composition 1

Wettable powder parts of 2-methoxy-N- (2,6-dimethylphenyl) -N- (2-oxx-3-oxoxolidinyl) ace^andTamide is milled with 2 parts of lauryl sulfate, 3 parts of trisulphineignin sulphate and 45 parts of finely dispersed kaolinite until the mean particle size is less than 5 μτη. Those who obtained the powder are diluted with water prior to use to an active compound concentration of 0.01-5%. The resulting spray liquid can be applied by spraying on the leaves of the plants, or it serves to water the root portion of the plants.

Example - the means 2

Granulate

0.5 parts by weight of binder (or ionic surfactant is sprayed onto the 94.5 parts by weight of quartz sand in a tumbler mixer and mixed thoroughly. Then 5 parts by weight of 2-methoxy-N- (2,6- diethylphenyl) -N- (2-oxo-3-oxazolidinyl) ace^,tamid and thorough mixing is continued until granulated particles of 0.3-0.7 mm are obtained. The granulate can be incorporated into the soil around the treated soil.

Example 1

2-Nethoxy-N- (2,6-dimethylphenyl) -N-

- (2-oxo-X-xxxazolidinyl) acetamide

11.8 g (0.037 5 mol) of 2-chloromethyl-2- (non-methoxyacetyl) -2- (2,6-dimethylphenyl) hydraolecarboxylate are added in portions to a suspension of 2.0 g of sodium hydride (in form (55% by weight in mineral oil) in 100 ml of absolute toluene at room temperature and under nitrogen. The reaction temperature gradually increased during the addition up to -40 ° C. When the addition is complete, the mixture is stirred after. The reaction was cooled to 10 ° C for 30 minutes^CUnreacted sodium hydride is then destroyed with ethainol, the solution is washed with water, dried over magnesium sulfate and the solvent is removed in vacuo to give 2-methoxy-N- (2,6-dimethylphenyl) -N- (2-oxo-3-oxazolidinyl) acetamide, which is recrystallized from ethanol to give colorless crystals, m.p. 103-104 ° C.

Example 1 -ad 1a

2-Chloroethyl 1-2- (methoxyacetyl) -2- (2,6-dimethylphenyl) hydrahydic acid^,boxylate

The starting material used in Example 1 was obtained as follows:

14.7 g (0.06 mol) of 2-chloroethyl-2-

- (2,6-dimethylphenyl) hydrazinecarboxylate a

16.2 g (0.1 mol) of non-methoxyacetic anhydride of formula [(CH 3 OCH 2 CO) 2 O 3 are stirred in 100 ml of dry toluene for one hour at -80 ° C. After cooling, the solution was washed with water, then with 5% aqueous hydrogen carbonate solution and then with water again.

The solution was dried with magnesium sulfate and the solvent removed in vacuo to give 2-chloroethyl 1- (methoxyacetyl) -2- (2,6-dimethylienyl) hydrazinecarboxylate.

Example 1b

2-Chloromethyl-2- (2,6-diethylphenyl) hydrazinecarboxylate

To a mixture of 127 g (0.935 mol) of 2,6-dimethyl-2,4-dimethylphenylhydrazine, 102.5 g (1.3 mol) of pyridine and 400 ml of water are added at 0-5 ° C.

133.5 g (0.935 mol) of beta-chloroethyl chloroformate After the addition is complete, the mixture is stirred for two hours at room temperature, the precipitate formed is filtered off, washed with water and dried. (2,6-dimethylphenyl) hydrazinecarboxylate is recrystallized from toluene to give colorless crystals, m.p. 74-75 ° C.

The preferred method of Example 1, 1a, 1b is as follows:

Example 2

2-Methoxy-N- (2,6-dimethylphenyl) -N- (2-oxo-3-oxazolidinyl) acetamide

236.1 g (0.75 mol) of 2-chloroethyl 2- (methoxyacetyl) -2- (2,6-dimethylphenyl) hydrazinecarboxylate, 375 ml of xylene and 187 ml of water are stirred with cooling while 82, 5 ml (0.82 mol) of aqueous sodium hydroxide solution containing about 0.4 g of sodium hydroxide per ml, at a rate to maintain an internal temperature of about 20 ° C. After complete addition, the mixture was stirred for 1 hour at 20 ° C and for 2 hours at 0 ° C. The solid was filtered, washed with water (150 ml) and dried to give 2-methoxy-N- (2,6-dimethylphenyl) -N- (2-oxo-3-oxazolidinyl) acetamide as a slightly colored solid. m.p. 102-103 ° C.

200 g (0.825 mol) of 2-chloroethyl 2- (2,6-dimethylphenyl) hydrazinecarboxylate in 500 ml of xylene is heated to 80 ml. ^CC and added to a warm (80 ° C) solution of 2-methoxyacetyl chloride in 250 ml of xylene prepared in silo by treating 73.5 g (0.826 mol) of 2-methoxy-acetic acid in 250 ml of xylene,

107.1 g (0.9 mol) of thionyl chloride at 80 ° C for two hours. Smě :; The mixture is heated at 80 DEG C. for 30 minutes and then worked up as described in Example 1a.

Example 2b

2-Chloroethyl-2- (2,6-dimethyl-phenyl) -hrazole inkarbutyl

A mixture of 17.7 g (0.1 mol) of 2,6-dimethylphenylhydrazine hydrochloride, 21.2 g (0.2 mol) of sodium carboxylate in 50 ml of water and 50 ml of xylene is stirred for 30 minutes at room temperature and then cooled. to 5 ^C'C. 14.3 g (0.1 mol) of 2-chloroethyl chloroformate were then added over one hour, maintaining the temperature at 5 ° C. The mixture is stirred at 5 ° C for an additional hour, at the end of which 100 ml of water are added, the precipitate formed is filtered off, washed with water and dried. Further processing is the same as described in Example 1b.

In a similar manner as described in Examples 1 and 2, the following compounds of Formula I were also prepared.

Example 2a

2-chloroethyl 2- (methoxyacetyl) -2- (2,6-dimethylphenyl) hydrazinecarboxylate

Example number R7

Rto Melting point (° C)

Re

Rg

<td> 3</td><td>СНз</td><td>СНз</td><td>н</td><td>СН2ОС2Н5</td>

<td> 4</td><td>СНз</td><td>С1</td><td>н</td><td>CH2OCH3</td>

<td> 5</td><td>СНз</td><td>СНз</td><td>н</td><td>ώ</td>

<td> 6</td><td>СНз</td><td>СНз</td><td>4-С1</td><td>СНгОСНз</td>

<td> 11</td><td>СНз</td><td>СНз</td><td>Н</td><td>СНгОСН [СН5) 2</td>

<td> 12</td><td>СНз</td><td>С1</td><td>н</td><td>СНгОСН (СНз) 2</td>

<td> 13</td><td>СНз</td><td>С1</td><td>н</td><td>ТУ^в</td>

<td> 19</td><td>СНз</td><td>СНз</td><td>н</td><td>УУ</td>

Cl Cl

H

CH2OCH5 to 64 to 100

190 to 191

107 to 109

166 to 167

119 to 120

Cl * Cl H

<img file="CS249506B2_D0005.tif" />

173 to 174

<td>Example number</td><td>R7</td><td>R8</td><td>R9</td><td>R10</td><td>Melting point (° C)</td>

<td> 24</td><td>СНз</td><td>СНз</td><td>4-СНз</td><td>СНгОСНз</td><td>oil</td>

<td> 26</td><td>СНз</td><td>СНз</td><td>3-С1</td><td>СНгОСНз</td><td>90 to 92</td>

<td> 27</td><td>СНз</td><td>СНз</td><td>З-Вг</td><td>СНгОСНз</td><td>96 to 97</td>

<td> 29</td><td>СНз</td><td>СНз</td><td>З-Вг</td><td>Ίύ</td><td>145 to 148</td>

<td> 30</td><td>СНз</td><td>Вт</td><td>4-СНз</td><td>СНгОСНз</td><td>125 to 126 '</td>

<td> 32</td><td>СНз</td><td>Вг</td><td>4-СНз</td><td>ILi</td><td>193 to 194</td>

<td> 33</td><td>СНз</td><td>СНз</td><td>Н</td><td>СНОСНз СНз</td><td>90 to 94</td>

<td> 34</td><td>СНз</td><td>СНз</td><td>Н</td><td>1__________i</td><td>149 to 152</td>

<td> 36</td><td>СНз</td><td>СНз</td><td>4-С1</td><td>L у</td><td>164 to 165</td>

<td> 37</td><td>С₂Н5</td><td>СаНз</td><td>Н</td><td>СН2ОСН5</td><td>109 to 112</td>

<td> 38</td><td>СНз</td><td>СНз</td><td>Н</td><td>СНгОСзН7 (п)</td><td>oil</td>

<td> 39</td><td>СНз</td><td>СНз</td><td>Н</td><td>CH 2 OC 9 H (n)</td><td></td>

<td> 40</td><td>СНз</td><td>СНз</td><td>Н</td><td>СН2ОСН — С2Н5 СНз</td><td></td>

<td> 46</td><td>С? Н5</td><td>С2Н5</td><td>Н</td><td>О.</td><td>142 to 144</td>

<td> 48</td><td>Вг</td><td>Вг</td><td>Н</td><td>CH2OCH3</td><td>150 to 152</td>

<td> 49</td><td>С1</td><td>С1</td><td>4-С1</td><td>СНгОСНз</td><td>128 to 129</td>

<td> 50</td><td>С2Н5</td><td>С2Н5</td><td>4-С1</td><td>СНгОСНз</td><td>114 to 116</td>

<td> 51</td><td>Вг</td><td>С1</td><td>4-СНз</td><td>СНгОСНз</td><td>131 to 134</td>

<td> 52</td><td>СНз</td><td>С2Н5</td><td>Н</td><td>СНгОСНз</td><td>96 to 98</td>

<td> 53</td><td>СНз</td><td>СНз</td><td>4-Вг</td><td>СНгОСНз</td><td>137 to 138</td>

OBJECT OF THE INVENTION