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filingDate 2005-08-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2006-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AR-050692-A1
titleOfInvention DERIVATIVES OF TRIAZOLOPIRIDINILSULFANILO AS QUINASA MAP P38 INHIBITORS; PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM AND THEIR USE IN THE MANUFACTURE OF MEDICINES FOR THE TREATMENT OF DISEASES MEDIATED BY TNF OR P38
abstract Use of this compound in the treatment of a disease, disorder or condition mediated by TNF, or a disease, disorder or condition mediated by p38, in particular allergic and non-allergic diseases of the respiratory tract, more particularly obstructive or inflammatory diseases of the airways, preferably chronic obstructive pulmonary disease. Claim 1: A compound of formula (1), or a pharmaceutically acceptable salt and / or solvate (including hydrate), wherein: R1 is CH3, S (O) pCH3, S (O) pCH2CH3, CH2CH3, H or CH2S (O) pCH3; R1a is CH3 or CH2CH3, where each CH3 and CH2CH3 is optionally substituted with one or more hydroxy substituents; R2 is heteroaryl, heterocyclyl, aryl, or carbocyclyl; R3 is heteroaryl, heterocyclyl, aryl, carbocyclyl or R7; R7 is C1-6 alkyl (optionally substituted with one or more substituents independently selected from OH, halo, NR5R6, C1-6 alkoxy, -S (O) C1-6 alkyl, CO2H, CONR5R6, heteroaryl, heterocyclyl, aryl, carbocyclyl, aryloxy , carbocyclyloxy, heteroaryloxy and heterocyclyloxy); p is 0, 1 or 2; each of R5 and R6 is independently selected from H and C1-4 alkyl, said C1-4 alkyl being optionally substituted with one or more substituents independently selected from OH and halo; or R5 and R6, together with the nitrogen to which they are attached form a piperazinyl, piperidinyl, morpholinyl or pyrrolidinyl group, (each of said piperazinyl, piperidinyl, morpholinyl and pyrrolidinyl being optionally substituted with one or more OH); each "aryl" independently means phenyl or naphthyl, said phenyl or naphthyl being optionally substituted with one or more substituents independently selected from halo, -CN, -CO2H, OH, CONR5R6, NR5R6, R8 and R9; each R8 is independently selected from C1-6 alkyl, C1-6 alkoxy, -CO2C1-6 alkyl, -S (O) C1-6 alkyl, -C1-6 alkyl and C3-7 cycloalkyl; each R8 is optionally substituted with one or more substituents independently selected from: C1-6 alkoxy (optionally substituted with one or more substituents independently selected from OH, halo, CO2H, CONR5R6 and NR5R6); S (O) C 1-6 palkyl (optionally substituted with one or more substituents independently selected from OH, halo, CO2H, CONR5R6 and NR5R6); OH; halo; NR5R6; CO2H; CONR5R6; and R9; R9 is heteroaryl2, heterocyclyl2, aryl2, carbocyclyl2, aryl2oxy, carbocyclyloxy2, heteroaryl2oxy or heterocyclyl2oxy; "aryl 2" means phenyl or naphthyl, said phenyl or naphthyl being optionally substituted with one or more substituents independently selected from halo, -CN, -CO2H, OH, NR5R6 and CONR5R6; "Carbocyclyl" means a mono or bicyclic ring system, saturated or partially unsaturated C3-10 in the ring, optionally substituted with one or more substituents independently selected from halo, -CN, -CO2H, OH, NR5R6, CONR5R6, R8 and R9; "Carbocyclyl2" means a mono or bicyclic ring system, saturated or partially unsaturated C3-10 in the ring, optionally substituted with one or more substituents independently selected from halo, -CN, -C0H, NR5R6, OH and CONR5R6; each "heterocyclyl," and "heterocyclyl2", independently, means a saturated or partially unsaturated mono or bicyclic group of 3 to 10 members comprising 1 to 4 ring heteroatoms independently selected from N, O, and S; each "heteroaryl" and each "heteroaryl2" independently means a mono or bicyclic aromatic group of 5 to 10 members comprising from 1 to 4 heteroatoms in the ring independently selected from N, O and S (where the total number of S atoms in the ring does not exceed 1, and the total number of O atoms in the ring does not exceed 1); each "heterocyclyl" group and each "heteroaryloyl" group is, independently, optionally substituted at one or more carbon atoms in the ring with one or more substituents independently selected from halo, -CN, -CO2H, OH, NR5R6, CONR5R6, R8 and R9, and optionally substituted on one or more ring nitrogen atoms with one or more substituents independently selected from H and C1-6 alkyl; and each ôheterocyclyl2ö group and each ôheteroaryl2ö group is, independently, optionally substituted on one or more carbon atoms in the ring with one or more substituents independently selected from halo, -CN, -CO2H, NR5R6, OH and CONR5R6, and optionally substituted on one or more ring nitrogen atoms with one or more substituents independently selected from H and C1-6 alkyl.
priorityDate 2004-08-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 68.