http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2319302-T3

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filingDate 2004-07-26^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2009-05-06^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f42a239eb21188d9c8e199155f178a90
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_629bc941f36d904e4ef6593b4c3306e0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ccee479c069450c11ef582caaea2bb3a
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8c9fde6dbfcb67767d5cf7871d36156a
publicationDate 2009-05-06^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2319302-T3
titleOfInvention INHIBITORS OF TIENOPIRIDINA AND FUROPIRIDINA KINASA.
abstract A compound of formula (I) ** see formula ** or a therapeutically acceptable salt thereof, wherein R 1 is selected from the group consisting of alkoxyalkynyl, alkoxycarbonylalkenyl, alkoxycarbonyl-alkyl, alkynyl, aryl, arylalkyl, alkoxy-alkynyl, arylsulfanylalkyl , carboxyalkenyl, carboxyalkyl, carboxyalkynyl, cyanoalkyl, cycloalkylalkynyl, formilalquenilo, halo, heteroaryl, heteroarylalkynyl, heteroarilcarbonilalquenilo, hetero-arylcarbonylalkyl, heterocyclyl, heterocyclyl-alkyl, heterocyclyl alkynyl, heterocyclylcarbonyl-alkenyl, hydroxyalkenyl, hydroxyalkyl, hydroxyalkynyl, NR a R b, (NR a R b) alkenyl, (NR to R b) alkyl, (NR to R b) alkyl, (NR to R b) carbonylalkenyl, (NR to R b) carbonyl alkyl, and nitro; R 2 is selected from the group consisting of hydrogen and alkyl; R 3 is selected from the group consisting of halo, aryl, heteroaryl, and heterocyclyl, where aryl, heteroaryl, and heterocyclyl are optionally substituted with one, two, or three substituents independently selected from the group consisting of alkoxy, alkyl, aryl, cyano, halo, haloalkoxy, haloalkyl, heteroaryl, hydroxyalkyl, LR 4, and NR a R b; provided that at least two of the three substituents are different from LR 4; L is selected from the group consisting of O, NR 5 C (O) (CH2) m, NR 5 SO2, and (CH2) mN (R 5) C (O) N (R 5) (CH2) a, where myn they are 0 1 and where each group is represented with its right end anchored to R 4; R 4 is selected from the group consisting of aryl, arylalkyl, heteroaryl, and heterocyclyl; R 5 and R 6 are hydrogen; R a and R b are independently selected from the group consisting of hydrogen, alkyl, alkylcarbonyl, alkylsulfonyl, cycloalkyl, heterocyclylcarbonyl, (NR to R b) alkylcarbonyl, and R a and R d are independently selected from the group consisting of hydrogen, and alkyl, wherein heteroaryl is selected from benzimidazolyl, benzoxadiazolyl, benzoxazolyl, benzofuranyl, benzisoxazolyl, benzothiazolyl, benzothienyl, cinnolinyl, dibenzofuranyl, furanyl, furyl, imidazolyl, indazolyl, indolyl, isoxazolyl, isoquinolinyl, isothiazolyl, naphthyridinyl, oxadiazolyl, oxadiazolyl, oxazolyl, pyridinyl, pyridazinyl , pyrimidinyl, pyrazinyl, pyrazolyl, pyrrolyl, quinolinyl, thiazolyl, thienopyridinyl, thienyl, triazolyl, thiadiazolyl, and triazinyl, and wherein heterocyclyl is selected from azetidinyl, benzodioxolyl, benzothiazolyl, diazepanyl, dihydroindolyl, dihydroisoindolyl, dihydropyridinyl, 1,3-dioxanyl, 1,4-dioxanyl, 1,3-dioxolanyl, isoindolinyl, mo rfolinyl, piperazinyl, pyrrolidinyl, tetrahydropyridinyl, piperidinyl, and thiomorpholinyl, diazepinyl, imidazolidinyl, morpholinyl.
priorityDate 2003-07-24^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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