http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2349331-T3
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_12a9e9ce63eb0bbf3658453fb50a6d9b |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-0812 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-88 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-70 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D235-26 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D235-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-64 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P13-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P7-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P27-02 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-381 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D235-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-423 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4162 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4184 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C311-21 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-88 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-70 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-64 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-404 |
| filingDate | 2008-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2010-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_49b65f0b283407d8c9ce49db5554257d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_228101d75caf3d1d347888e562589f0e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_149a4e5568d70048a9d45144cf6f8292 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7f30c44457c387c63fcbfd88be2dde7d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_797b129acf455e88789e98c6135f77dc http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_252c0951050af89ae0547ab6a72c3441 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_802d76dfde9f8c32f38d2352c00ee1eb |
| publicationDate | 2010-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-2349331-T3 |
| titleOfInvention | NEW ARILSULFONILGLICINAS REPLACED, ITS OBTAINING AND ITS USE AS PHARMACEUTICAL COMPOSITIONS. |
| abstract | Compounds of the general formula (I) ** (See formula) ** in which 5 R indicates a group of the formula ** (See formula) ** in which R1 means H, C1-6 alkyl or a group of the formula ** (See formula) ** in which the above-mentioned C1-6 alkyl group for R1 may be substituted by (C1-6 alkyl) -carbonyloxy, (C1-6 alkoxy) carbonyloxy, C1-6 alkoxy, hydroxy, amino, (C1-3 alkyl) -amino, di (C1-3 alkyl) -amino, pyrrolidin-1-yl, piperidin-1-yl, morpholin-4-yl, piperazin-1-yl, 4- ( C1-3 alkyl) -piperazin-1-yl, aminocarbonyl, (C1-3 alkyl) -aminocarbonyl, di (C1-3 alkyl) aminocarbonyl, pyrrolidin-1-yl-carbonyl, piperidin-1-ylcarbonyl, morpholin-4 -yl-carbonyl, piperazin-1-yl-carbonyl, 4- (C1-3alkyl) -piperazin-1-yl-carbonyl, tetrahydrofuran-3yl-oxy, (C1-3alkyl) -amino-C1-3alkyloxy, di (C1-3 alkyl) C1-3 amino-alkyloxy, pyrrolidin-1-yl-C1-3 alkyloxy, piperidin-1-yl-C1-3 alkyloxy, morpholin-4-yl-C1-3 alkyloxy, 5 zin pipette -1-yl-C 1-3 alkyloxy or 4- (C 1-3 alkyl) -piperazin-1-yl C1-3 alkyloxy, R2 and R3 independently of each other mean halogen, C1-3 alkyl, C2-4 alkynyl, C1-3 perfluoralkyl, C1-3 perfluoralkoxy, C1-3 alkoxy, cyano, nitro or hydroxy and 10 A means CH or N, and the heterocyclic group ** (See formula) ** means a group of the formulas ** (See formula) ** ** (See formula) ** in which the heterocycles of the formulas (Ia), ( Ib), (Ic), (Ie), (If), (Ig), (Ii) and (In) just mentioned may in each case be optionally substituted in the carbon atoms of the 5-link ring by one or two groups chosen from C1-3 alkyl, amino C1-3 alkyl, hydroxy C1-3 alkyl, cyano, perfluoralkyl C1-3, cycloalkyl C3-6, alkynyl C2-4, alkenyl C2-4, (alkyl C1-3) -carbonyl, (perfluoralkyl C1-3) 10 carbonyl, carboxyl, (C1-3 alkyloxy) -carbonyl, C1-3 carboxyalkyl, aminocarbonyl, (C1-3 alkyl) -aminocarbonyl or di (C1-3 alkyl) -aminocarbonyl, said groups can be identical or different and each carbon atom can carry only one group varies, and the heterocyclic group of the aforementioned formula (Ib) may optionally be substituted on the nitrogen atom of the 5-link ring by methyl or hydroxycarbonylmethyl, and where R4 means H, cyano, C1- alkyl 6, phenyl-C 1-6 alkyl, phenylsulfonyl-C 1-6 alkyl, (C 1-6 alkyl) -carbonyl, carboxyl, (C 1-6 alkoxy) -carbonyl phenylcarbonyl, phenyl- (C 1-6 alkyl) carbonyl, 5-chloro -1H-indole-2-yl-carbonyl, aminocarbonyl, (C1-6 alkyl) -aminocarbonyl, di (C1-6 alkyl) -aminocarbonyl, (C3-6 cycloalkyl) -aminocarbonyl, N- (C3-6 cycloalkyl) N (C1-6 alkyl) -amino-carbonyl, aryl-amino-carbonyl, N-oxypyridylamino-carbonyl, (cycloalkylene of 4 to 7 links) imino-carbonyl optionally substituted by hydroxy or (C1-3 alkyl) -aminocarbonyl, morpholin -4-yl-carbonyl, piperazin-1-yl-carbonyl, 4- (C1-3alkyl) -piperazin-1-yl-carbonyl, (piperazin-2-on-4-yl) -carbonyl, aminocarbonylcarbonyl, (alkyl C1-3) -aminocarbonylcarbonyl, di (C1-3alkyl) -amino carbonylcarbonyl, pyrrolidin-1-ylcarbonylcarbonyl, piperidin-1-ylcarbonylcarbonyl, morpholin-4-ylcarbonylcarbonyl, piperazin-1-ylcarbonylcarbonyl, 4-methylpiperazin-1-ylcarbonylcarbonyl, (C1-3 alkyl) -sulfonyl , phenyl- (C1-3 alkyl) -sulfonyl or phenylsulfonyl optionally substituted in the phenyl moiety by one or two chlorine atoms, said (C1-6 alkyl) -aminocarbonyl, di- (C1-6 alkyl) -aminocarbonyl and N groups - (C3-6 cycloalkyl) -N- (C1-6 alkyl) -aminocarbonyl mentioned above in the definition of R4 may in each case be substituted by alkyl by aryl, (C1-3 alkyl) -amino, di (alkyl C1-3) -amino, (C3-6 cycloalkyl) amino, N- (C3-6 cycloalkyl) -N- (C1-6 alkyl) -amino, pyrrolidin1-yl, piperidin-1-yl, morpholin-4-yl , piperazin-1-yl, 4-methyl-piperazin-1-yl or (C1-3 alkyl) -aminocarbonyl and in which the aryl group mentioned above in the definition of R4 is a 6-link aromatic system that may contain from 0 to 3 nitrogen atoms and can be substituted or by nitro. |
| priorityDate | 2007-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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