Chemical compounds
Abstract
A compound of formula (I) (see formula) wherein: R 1 and R 2 are independently selected from hydrogen, halo, nitro, cyano, hydroxy, trifluoromethoxy, amino, carboxy, carbamoyl, mercapto, sulfamoyl, C1 - 6 C2 - 6 alkynyl C2 - 6 alkoxy C1 - 6 alkanoyl C1 - 6 alkanoyloxy C1 - 6, N- (C1 - 6) amino, N, N- (C1 - 6) 2amino, alkanoylamino C1 - 6, N- (C1 - 6) carbamoyl, N, N- (C1 - 6) 2carbamoílo, [C1 - 6] S (O) a wherein a is 0 to 2, alkoxycarbonyl C1 - 6, N- (C1 - 6) sulphamoyl, N, N- (C1 - 6) 2sulfamoílo, [C1 - 6] alkylsulfonylamino, carbocyclyl or heterocyclyl; wherein R 1 and R 2 independently of one another, may be optionally substituted on carbon by one or more R 8 and wherein if said heterocyclyl contains an -NH- moiety that nitrogen may be optionally substituted by a group selected from R 9; X 1, X 2 and X 3 are independently = N- or = CR 10 -; R 3 and R 10 are independently selected from hydrogen, halo, nitro, cyano, hydroxy, trifluoromethoxy, amino, carboxy, carbamoyl, mercapto, sulfamoyl, C1 - 6 C2 - 6 alkynyl C2 - 6 alkoxy C1 - 6 alkanoyl C1 - 6 alkanoyloxy C1 - 6, N- (C1 - 6) amino, N, N- (C1 - 6) 2amino, alkanoylamino C1 - 6, N- (C1 - 6) carbamoyl, N , N- (C1 - 6) 2carbamoílo, [C1 - 6] s (O) a wherein a is 0 to 2, alkoxycarbonyl C1 - 6, N- (C1 - 6) sulphamoyl, N, N- (C1 - 6) 2sulfamoílo [C1 - 6] sulfonylamino, carbocyclyl-R 11 - or heterocyclyl-R 12 -; wherein R 3 and R 10 independently of one another, may be optionally substituted on carbon by one or more R 13 and wherein if said heterocyclyl contains an -NH- moiety that nitrogen may be optionally substituted by a group selected from R 14; R 4 is ...
Term
No projected expiry on record.
- Priority
- Filed
- Granted
- Today
37 members in 25 offices
Priority claims2
| Document | Office | Kind | Date |
|---|---|---|---|
| 65357505 | United States of America | P | |
| 74213805 | United States of America | P |
Members37
| Document | Office | Kind | |
|---|---|---|---|
| AU2006215386A1 | Australia | A1 | |
| CA2597813A1 | Canada | A1 | |
| WO2006087530A1 | World Intellectual Property Organization (WIPO) | A1 | |
| MX2007009843A | Mexico | A | |
| NO20073788L | Norway | L | |
| KR20070103773A | Republic of Korea | A | |
| EP1853588A1 | European Patent Office (EPO) | A1 | |
| IL185063A0 | Israel | A0 | |
| IL185063D0 | Israel | D0 | |
| CN101119988A | China | A | |
| EP1853588B1 | European Patent Office (EPO) | B1 | |
| AT398613TThis record | Austria | T | |
| ATE398613T1 | Austria | T1 | |
| US2008176872A1 | United States of America | A1 | |
| DE602006001515D1 | Germany | D1 | |
| JP2008530190A | Japan | A | |
| PT1853588E | Portugal | E | |
| ZA200706493B | South Africa | B | |
| DK1853588T3 | Denmark | T3 | |
| HK1114375A1 | Hong Kong, China | A1 | |
| SI1853588T1 | Slovenia | T1 | |
| PL1853588T3 | Poland | T3 | |
| ES2308731T3 | Spain | T3 | |
| RU2007134396A | Russian Federation | A | |
| AU2006215386B2 | Australia | B2 | |
| BRPI0607455A2 | Brazil | A2 | |
| NZ561525A | New Zealand | A | |
| RU2405780C2 | Russian Federation | C2 | |
| UA93198C2 | Ukraine | C2 | |
| IL185063A | Israel | A | |
| US8129403B2 | United States of America | B2 | |
| US2012122892A1 | United States of America | A1 | |
| JP5001179B2 | Japan | B2 | |
| CN101119988B | China | B | |
| CY1108275T1 | Cyprus | T1 | |
| KR101362621B1 | Republic of Korea | B1 | |
| CA2597813C | Canada | C |
1 legal event, as the office reported them to INPADOC
Events
| Event | Code | |
|---|---|---|
| Publication of translation of european patent specificationUEP | UEP |
Numbers
- Application
- 6709750
Titles2
- German
- CHEMISCHE VERBINDUNGEN
- English
- CHEMISCHE VERBINDUNGEN
Classification
- CPC, 18
- C07D473/32
- C07D403/04
- A61P9/10
- C07D401/14
- A61P13/12
- A61P17/06
- C07D471/04
- A61P19/02
- C07D487/04
- A61P19/08
- A61P27/02
- A61P29/00
- A61P35/00
- A61P35/02
- A61P35/04
- A61P37/06
- A61P43/00
- A61K31/4155
- IPC, 3
- C07D403 04
- A61K31 4155
- A61P35 00