JP2014511869A5 - - Google Patents
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- Publication number
- JP2014511869A5 JP2014511869A5 JP2014504251A JP2014504251A JP2014511869A5 JP 2014511869 A5 JP2014511869 A5 JP 2014511869A5 JP 2014504251 A JP2014504251 A JP 2014504251A JP 2014504251 A JP2014504251 A JP 2014504251A JP 2014511869 A5 JP2014511869 A5 JP 2014511869A5
- Authority
- JP
- Japan
- Prior art keywords
- pyrazole
- carboxamide
- pyrimidin
- formula
- compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 150000001875 compounds Chemical class 0.000 claims 29
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 16
- 125000000623 heterocyclic group Chemical group 0.000 claims 13
- 229910052739 hydrogen Inorganic materials 0.000 claims 13
- 239000001257 hydrogen Substances 0.000 claims 13
- 150000003839 salts Chemical class 0.000 claims 11
- 125000003710 aryl alkyl group Chemical group 0.000 claims 10
- 125000003118 aryl group Chemical group 0.000 claims 10
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims 10
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 9
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 6
- 150000002431 hydrogen Chemical group 0.000 claims 4
- 229910052757 nitrogen Inorganic materials 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 239000003814 drug Substances 0.000 claims 3
- 125000001072 heteroaryl group Chemical group 0.000 claims 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 239000002246 antineoplastic agent Substances 0.000 claims 2
- 229940127089 cytotoxic agent Drugs 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 150000002367 halogens Chemical group 0.000 claims 2
- 125000005842 heteroatom Chemical group 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- YNJNLGYPTQPTPW-UHFFFAOYSA-N 1-(6-methoxypyridin-3-yl)-5-pyrimidin-4-ylpyrazole-3-carboxylic acid Chemical compound C1=NC(OC)=CC=C1N1C(C=2N=CN=CC=2)=CC(C(O)=O)=N1 YNJNLGYPTQPTPW-UHFFFAOYSA-N 0.000 claims 1
- YIGPUXRGBBZKJW-UHFFFAOYSA-N 1-tert-butyl-5-(2-methoxypyrimidin-4-yl)pyrazole-3-carboxamide Chemical compound COC1=NC=CC(C=2N(N=C(C=2)C(N)=O)C(C)(C)C)=N1 YIGPUXRGBBZKJW-UHFFFAOYSA-N 0.000 claims 1
- RFJQYCNMCJJJSG-UHFFFAOYSA-N 1-tert-butyl-5-(2-methylsulfanylpyrimidin-4-yl)pyrazole-3-carboxamide Chemical compound CSC1=NC=CC(C=2N(N=C(C=2)C(N)=O)C(C)(C)C)=N1 RFJQYCNMCJJJSG-UHFFFAOYSA-N 0.000 claims 1
- NPAPHHQDTZZLSK-UHFFFAOYSA-N 1-tert-butyl-5-(2-morpholin-4-ylpyrimidin-4-yl)-n-phenylpyrazole-3-carboxamide Chemical compound CC(C)(C)N1N=C(C(=O)NC=2C=CC=CC=2)C=C1C(N=1)=CC=NC=1N1CCOCC1 NPAPHHQDTZZLSK-UHFFFAOYSA-N 0.000 claims 1
- LLSIYQYYVAAHEN-UHFFFAOYSA-N 1-tert-butyl-5-(2-phenoxypyrimidin-4-yl)-n-phenylpyrazole-3-carboxamide Chemical compound CC(C)(C)N1N=C(C(=O)NC=2C=CC=CC=2)C=C1C(N=1)=CC=NC=1OC1=CC=CC=C1 LLSIYQYYVAAHEN-UHFFFAOYSA-N 0.000 claims 1
- VZYACGCYABUZMD-UHFFFAOYSA-N 1-tert-butyl-5-(2-phenoxypyrimidin-4-yl)-n-propan-2-ylpyrazole-3-carboxamide Chemical compound CC(C)(C)N1N=C(C(=O)NC(C)C)C=C1C1=CC=NC(OC=2C=CC=CC=2)=N1 VZYACGCYABUZMD-UHFFFAOYSA-N 0.000 claims 1
- XWSQCSJHYIBIPB-UHFFFAOYSA-N 1-tert-butyl-5-(2-phenylpyrimidin-4-yl)pyrazole-3-carboxamide Chemical compound CC(C)(C)N1N=C(C(N)=O)C=C1C1=CC=NC(C=2C=CC=CC=2)=N1 XWSQCSJHYIBIPB-UHFFFAOYSA-N 0.000 claims 1
- NXUZHSNCDIAGAY-UHFFFAOYSA-N 1-tert-butyl-5-[2-(4-cyanophenoxy)pyrimidin-4-yl]-n-methylpyrazole-3-carboxamide Chemical compound CC(C)(C)N1N=C(C(=O)NC)C=C1C1=CC=NC(OC=2C=CC(=CC=2)C#N)=N1 NXUZHSNCDIAGAY-UHFFFAOYSA-N 0.000 claims 1
- DMLNFHDCCVVACO-UHFFFAOYSA-N 1-tert-butyl-5-[2-(4-cyanophenoxy)pyrimidin-4-yl]-n-phenylpyrazole-3-carboxamide Chemical compound CC(C)(C)N1N=C(C(=O)NC=2C=CC=CC=2)C=C1C(N=1)=CC=NC=1OC1=CC=C(C#N)C=C1 DMLNFHDCCVVACO-UHFFFAOYSA-N 0.000 claims 1
- GLOLZXJNFUHZRR-UHFFFAOYSA-N 1-tert-butyl-5-[2-(4-cyanophenoxy)pyrimidin-4-yl]-n-propan-2-ylpyrazole-3-carboxamide Chemical compound CC(C)(C)N1N=C(C(=O)NC(C)C)C=C1C1=CC=NC(OC=2C=CC(=CC=2)C#N)=N1 GLOLZXJNFUHZRR-UHFFFAOYSA-N 0.000 claims 1
- AXRBYRBXIFSKIF-UHFFFAOYSA-N 1-tert-butyl-5-[2-(4-piperazin-1-ylphenoxy)pyrimidin-4-yl]pyrazole-3-carboxamide Chemical compound CC(C)(C)N1N=C(C(N)=O)C=C1C1=CC=NC(OC=2C=CC(=CC=2)N2CCNCC2)=N1 AXRBYRBXIFSKIF-UHFFFAOYSA-N 0.000 claims 1
- JPXVJHYKCAPQRA-UHFFFAOYSA-N 1-tert-butyl-5-[2-(dimethylamino)pyrimidin-4-yl]-n-methylpyrazole-3-carboxamide Chemical compound CC(C)(C)N1N=C(C(=O)NC)C=C1C1=CC=NC(N(C)C)=N1 JPXVJHYKCAPQRA-UHFFFAOYSA-N 0.000 claims 1
- JGLZQEWJZMTROM-UHFFFAOYSA-N 1-tert-butyl-5-[2-(dimethylamino)pyrimidin-4-yl]-n-phenylpyrazole-3-carboxamide Chemical compound CN(C)C1=NC=CC(C=2N(N=C(C=2)C(=O)NC=2C=CC=CC=2)C(C)(C)C)=N1 JGLZQEWJZMTROM-UHFFFAOYSA-N 0.000 claims 1
- KHJXLLUKAIABND-UHFFFAOYSA-N 1-tert-butyl-5-[2-(dimethylamino)pyrimidin-4-yl]-n-propan-2-ylpyrazole-3-carboxamide Chemical compound CC(C)(C)N1N=C(C(=O)NC(C)C)C=C1C1=CC=NC(N(C)C)=N1 KHJXLLUKAIABND-UHFFFAOYSA-N 0.000 claims 1
- STVXWMPMCBWAQK-UHFFFAOYSA-N 1-tert-butyl-5-[2-(dimethylamino)pyrimidin-4-yl]pyrazole-3-carboxamide Chemical compound CN(C)C1=NC=CC(C=2N(N=C(C=2)C(N)=O)C(C)(C)C)=N1 STVXWMPMCBWAQK-UHFFFAOYSA-N 0.000 claims 1
- PMVLFBLYAWKVTH-UHFFFAOYSA-N 1-tert-butyl-n-methyl-5-(2-phenoxypyrimidin-4-yl)pyrazole-3-carboxamide Chemical compound CC(C)(C)N1N=C(C(=O)NC)C=C1C1=CC=NC(OC=2C=CC=CC=2)=N1 PMVLFBLYAWKVTH-UHFFFAOYSA-N 0.000 claims 1
- NWLNDDCQBDCBGL-UHFFFAOYSA-N 2-[(3-methoxyphenyl)methyl]-5-(2-methylpyrimidin-4-yl)pyrazole-3-carboxamide Chemical compound COC1=CC=CC(CN2C(=CC(=N2)C=2N=C(C)N=CC=2)C(N)=O)=C1 NWLNDDCQBDCBGL-UHFFFAOYSA-N 0.000 claims 1
- GNDPCMBWJSMFDH-UHFFFAOYSA-N 2-[(3-methoxyphenyl)methyl]-5-(2-oxo-1h-pyrimidin-6-yl)pyrazole-3-carboxamide Chemical compound COC1=CC=CC(CN2C(=CC(=N2)C=2N=C(O)N=CC=2)C(N)=O)=C1 GNDPCMBWJSMFDH-UHFFFAOYSA-N 0.000 claims 1
- -1 2-phenoxypyrimidin-4-yl Chemical group 0.000 claims 1
- SAZWNKNJUWDIKE-UHFFFAOYSA-N 3-(2-methylsulfanylpyrimidin-4-yl)-1h-pyrazole-5-carboxamide Chemical compound CSC1=NC=CC(C=2NN=C(C=2)C(N)=O)=N1 SAZWNKNJUWDIKE-UHFFFAOYSA-N 0.000 claims 1
- LPPNOCWWUZTIKG-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-1-(5-chloro-2-ethylphenyl)pyrazole-3-carboxamide Chemical compound CCC1=CC=C(Cl)C=C1N1C(C=2N=C(N)N=CC=2)=CC(C(N)=O)=N1 LPPNOCWWUZTIKG-UHFFFAOYSA-N 0.000 claims 1
- HOURAQDXNPRUJS-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-1-(5-chloro-2-methylphenyl)pyrazole-3-carboxamide Chemical compound CC1=CC=C(Cl)C=C1N1C(C=2N=C(N)N=CC=2)=CC(C(N)=O)=N1 HOURAQDXNPRUJS-UHFFFAOYSA-N 0.000 claims 1
- ZYDBWXADPWQAMI-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-ethylphenyl)pyrazole-3-carboxamide Chemical compound CCC1=CC=C(Cl)C=C1N1C(C(N)=O)=CC(C=2N=C(N)N=CC=2)=N1 ZYDBWXADPWQAMI-UHFFFAOYSA-N 0.000 claims 1
- MGCJYRVJINHYAP-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)pyrazole-3-carboxamide Chemical compound CC1=CC=C(Cl)C=C1N1C(C(N)=O)=CC(C=2N=C(N)N=CC=2)=N1 MGCJYRVJINHYAP-UHFFFAOYSA-N 0.000 claims 1
- IFXSYLKWEVEJIA-UHFFFAOYSA-N 5-(2-methylsulfanylpyrimidin-4-yl)-1-piperidin-4-ylpyrazole-3-carboxamide Chemical compound CSC1=NC=CC(C=2N(N=C(C=2)C(N)=O)C2CCNCC2)=N1 IFXSYLKWEVEJIA-UHFFFAOYSA-N 0.000 claims 1
- OHTRSASACJDQCI-UHFFFAOYSA-N 5-(2-methylsulfanylpyrimidin-4-yl)-2-piperidin-4-ylpyrazole-3-carboxamide Chemical compound CSC1=NC=CC(C2=NN(C(C(N)=O)=C2)C2CCNCC2)=N1 OHTRSASACJDQCI-UHFFFAOYSA-N 0.000 claims 1
- LXAHIOJOUKGSMV-UHFFFAOYSA-N 5-[2-(4-bromo-2-methoxyanilino)pyrimidin-4-yl]-n-(2,6-diethylphenyl)-1-[(4-methoxyphenyl)methyl]pyrazole-3-carboxamide Chemical compound CCC1=CC=CC(CC)=C1NC(=O)C1=NN(CC=2C=CC(OC)=CC=2)C(C=2N=C(NC=3C(=CC(Br)=CC=3)OC)N=CC=2)=C1 LXAHIOJOUKGSMV-UHFFFAOYSA-N 0.000 claims 1
- WBRIZQWMKIXWSK-UHFFFAOYSA-N 5-[2-(4-bromo-2-methoxyanilino)pyrimidin-4-yl]-n-(2,6-diethylphenyl)-1-methylpyrazole-3-carboxamide Chemical compound CCC1=CC=CC(CC)=C1NC(=O)C1=NN(C)C(C=2N=C(NC=3C(=CC(Br)=CC=3)OC)N=CC=2)=C1 WBRIZQWMKIXWSK-UHFFFAOYSA-N 0.000 claims 1
- SXSDYPDWRFRBOK-UHFFFAOYSA-N 5-[2-(4-bromo-2-methoxyanilino)pyrimidin-4-yl]-n-(2,6-diethylphenyl)-2-[(4-methoxyphenyl)methyl]pyrazole-3-carboxamide Chemical compound CCC1=CC=CC(CC)=C1NC(=O)C1=CC(C=2N=C(NC=3C(=CC(Br)=CC=3)OC)N=CC=2)=NN1CC1=CC=C(OC)C=C1 SXSDYPDWRFRBOK-UHFFFAOYSA-N 0.000 claims 1
- SIYHLKJVZNBAAO-UHFFFAOYSA-N 5-[2-(4-bromo-2-methoxyanilino)pyrimidin-4-yl]-n-(2,6-diethylphenyl)-2-methylpyrazole-3-carboxamide Chemical compound CCC1=CC=CC(CC)=C1NC(=O)C1=CC(C=2N=C(NC=3C(=CC(Br)=CC=3)OC)N=CC=2)=NN1C SIYHLKJVZNBAAO-UHFFFAOYSA-N 0.000 claims 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
- JPKZTKMCHHNHCK-UHFFFAOYSA-N N-hydroxy-3-(2-methylsulfanylpyrimidin-4-yl)-1H-pyrazole-5-carboxamide Chemical compound CSC1=NC=CC(C=2NN=C(C=2)C(=O)NO)=N1 JPKZTKMCHHNHCK-UHFFFAOYSA-N 0.000 claims 1
- 108091000080 Phosphotransferase Proteins 0.000 claims 1
- YNEYAILCVWIGMT-UHFFFAOYSA-N [1-(6-methoxypyridin-3-yl)-5-pyrimidin-4-ylpyrazol-3-yl]-(4-methylpiperazin-1-yl)methanone Chemical compound C1=NC(OC)=CC=C1N1C(C=2N=CN=CC=2)=CC(C(=O)N2CCN(C)CC2)=N1 YNEYAILCVWIGMT-UHFFFAOYSA-N 0.000 claims 1
- 230000001093 anti-cancer Effects 0.000 claims 1
- 238000011319 anticancer therapy Methods 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 230000000694 effects Effects 0.000 claims 1
- 238000000338 in vitro Methods 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- VRDMGEJYLOAERF-UHFFFAOYSA-N methyl 1-(6-methoxypyridin-3-yl)-5-(2-methylsulfanylpyrimidin-4-yl)pyrazole-3-carboxylate Chemical compound C=1C=C(OC)N=CC=1N1N=C(C(=O)OC)C=C1C1=CC=NC(SC)=N1 VRDMGEJYLOAERF-UHFFFAOYSA-N 0.000 claims 1
- NPDWZVIWNJMPPR-UHFFFAOYSA-N methyl 1-(6-methoxypyridin-3-yl)-5-pyrimidin-4-ylpyrazole-3-carboxylate Chemical compound C=1C=C(OC)N=CC=1N1N=C(C(=O)OC)C=C1C1=CC=NC=N1 NPDWZVIWNJMPPR-UHFFFAOYSA-N 0.000 claims 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 1
- ANWOMOBMTBNCGP-UHFFFAOYSA-N n-(2,6-diethylphenyl)-3-[2-(2-methoxyanilino)pyrimidin-4-yl]-1h-pyrazole-5-carboxamide Chemical compound CCC1=CC=CC(CC)=C1NC(=O)C1=NNC(C=2N=C(NC=3C(=CC=CC=3)OC)N=CC=2)=C1 ANWOMOBMTBNCGP-UHFFFAOYSA-N 0.000 claims 1
- GXEHCAYTZFZPQF-UHFFFAOYSA-N n-(2,6-diethylphenyl)-3-[2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]pyrimidin-4-yl]-1h-pyrazole-5-carboxamide Chemical compound CCC1=CC=CC(CC)=C1NC(=O)C1=NNC(C=2N=C(NC=3C(=CC(=CC=3)N3CCN(C)CC3)OC)N=CC=2)=C1 GXEHCAYTZFZPQF-UHFFFAOYSA-N 0.000 claims 1
- LNSLVWVMNZJSHN-UHFFFAOYSA-N n-(2,6-diethylphenyl)-3-[2-[4-[4-(2-hydroxyethyl)piperazin-1-yl]-2-methoxyanilino]pyrimidin-4-yl]-1h-pyrazole-5-carboxamide Chemical compound CCC1=CC=CC(CC)=C1NC(=O)C1=NNC(C=2N=C(NC=3C(=CC(=CC=3)N3CCN(CCO)CC3)OC)N=CC=2)=C1 LNSLVWVMNZJSHN-UHFFFAOYSA-N 0.000 claims 1
- UTWAVTYOSXACBH-UHFFFAOYSA-N n-(2,6-diethylphenyl)-5-[2-(2-methoxyanilino)pyrimidin-4-yl]-1-[(4-methoxyphenyl)methyl]pyrazole-3-carboxamide Chemical compound CCC1=CC=CC(CC)=C1NC(=O)C1=NN(CC=2C=CC(OC)=CC=2)C(C=2N=C(NC=3C(=CC=CC=3)OC)N=CC=2)=C1 UTWAVTYOSXACBH-UHFFFAOYSA-N 0.000 claims 1
- HVTSGLCSESUTKX-UHFFFAOYSA-N n-(2,6-diethylphenyl)-5-[2-(2-methoxyanilino)pyrimidin-4-yl]-1-methylpyrazole-3-carboxamide Chemical compound CCC1=CC=CC(CC)=C1NC(=O)C1=NN(C)C(C=2N=C(NC=3C(=CC=CC=3)OC)N=CC=2)=C1 HVTSGLCSESUTKX-UHFFFAOYSA-N 0.000 claims 1
- AIXGHQIUKRVEAX-UHFFFAOYSA-N n-(2,6-diethylphenyl)-5-[2-(2-methoxyanilino)pyrimidin-4-yl]-2-[(4-methoxyphenyl)methyl]pyrazole-3-carboxamide Chemical compound CCC1=CC=CC(CC)=C1NC(=O)C1=CC(C=2N=C(NC=3C(=CC=CC=3)OC)N=CC=2)=NN1CC1=CC=C(OC)C=C1 AIXGHQIUKRVEAX-UHFFFAOYSA-N 0.000 claims 1
- LPNFVFRZLDAJHS-UHFFFAOYSA-N n-(2,6-diethylphenyl)-5-[2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]pyrimidin-4-yl]-1-[(4-methoxyphenyl)methyl]pyrazole-3-carboxamide Chemical compound CCC1=CC=CC(CC)=C1NC(=O)C1=NN(CC=2C=CC(OC)=CC=2)C(C=2N=C(NC=3C(=CC(=CC=3)N3CCN(C)CC3)OC)N=CC=2)=C1 LPNFVFRZLDAJHS-UHFFFAOYSA-N 0.000 claims 1
- WZKSKKZREXLPGE-UHFFFAOYSA-N n-(2,6-diethylphenyl)-5-[2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]pyrimidin-4-yl]-1-methylpyrazole-3-carboxamide Chemical compound CCC1=CC=CC(CC)=C1NC(=O)C1=NN(C)C(C=2N=C(NC=3C(=CC(=CC=3)N3CCN(C)CC3)OC)N=CC=2)=C1 WZKSKKZREXLPGE-UHFFFAOYSA-N 0.000 claims 1
- YFPXKALYLATDPX-UHFFFAOYSA-N n-(2,6-diethylphenyl)-5-[2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]pyrimidin-4-yl]-2-methylpyrazole-3-carboxamide Chemical compound CCC1=CC=CC(CC)=C1NC(=O)C1=CC(C=2N=C(NC=3C(=CC(=CC=3)N3CCN(C)CC3)OC)N=CC=2)=NN1C YFPXKALYLATDPX-UHFFFAOYSA-N 0.000 claims 1
- ZFRAYIYRRCRCJI-UHFFFAOYSA-N n-(2,6-diethylphenyl)-5-[2-[4-[4-(2-hydroxyethyl)piperazin-1-yl]-2-methoxyanilino]pyrimidin-4-yl]-1-methylpyrazole-3-carboxamide Chemical compound CCC1=CC=CC(CC)=C1NC(=O)C1=NN(C)C(C=2N=C(NC=3C(=CC(=CC=3)N3CCN(CCO)CC3)OC)N=CC=2)=C1 ZFRAYIYRRCRCJI-UHFFFAOYSA-N 0.000 claims 1
- WYBUJUAJMUSILH-UHFFFAOYSA-N n-benzyl-1-tert-butyl-5-(2-phenoxypyrimidin-4-yl)pyrazole-3-carboxamide Chemical compound CC(C)(C)N1N=C(C(=O)NCC=2C=CC=CC=2)C=C1C(N=1)=CC=NC=1OC1=CC=CC=C1 WYBUJUAJMUSILH-UHFFFAOYSA-N 0.000 claims 1
- IUPQGRJRSIZORG-UHFFFAOYSA-N n-benzyl-1-tert-butyl-5-[2-(4-cyanophenoxy)pyrimidin-4-yl]pyrazole-3-carboxamide Chemical compound CC(C)(C)N1N=C(C(=O)NCC=2C=CC=CC=2)C=C1C(N=1)=CC=NC=1OC1=CC=C(C#N)C=C1 IUPQGRJRSIZORG-UHFFFAOYSA-N 0.000 claims 1
- KXJJQDWQTVXFCT-UHFFFAOYSA-N n-benzyl-1-tert-butyl-5-[2-(dimethylamino)pyrimidin-4-yl]pyrazole-3-carboxamide Chemical compound CN(C)C1=NC=CC(C=2N(N=C(C=2)C(=O)NCC=2C=CC=CC=2)C(C)(C)C)=N1 KXJJQDWQTVXFCT-UHFFFAOYSA-N 0.000 claims 1
- XMKDCEXITJWDAL-UHFFFAOYSA-N n-tert-butyl-1-(6-methoxypyridin-3-yl)-5-pyrimidin-4-ylpyrazole-3-carboxamide Chemical compound C1=NC(OC)=CC=C1N1C(C=2N=CN=CC=2)=CC(C(=O)NC(C)(C)C)=N1 XMKDCEXITJWDAL-UHFFFAOYSA-N 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 102000020233 phosphotransferase Human genes 0.000 claims 1
- 102000004169 proteins and genes Human genes 0.000 claims 1
- 108090000623 proteins and genes Proteins 0.000 claims 1
- 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 claims 1
- 210000004885 white matter Anatomy 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11161925.0 | 2011-04-11 | ||
| EP11161925 | 2011-04-11 | ||
| PCT/EP2012/056047 WO2012139930A1 (en) | 2011-04-11 | 2012-04-03 | Pyrazolyl-pyrimidine derivatives as kinase inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2014511869A JP2014511869A (ja) | 2014-05-19 |
| JP2014511869A5 true JP2014511869A5 (enExample) | 2015-05-21 |
| JP5976778B2 JP5976778B2 (ja) | 2016-08-24 |
Family
ID=46022177
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014504251A Expired - Fee Related JP5976778B2 (ja) | 2011-04-11 | 2012-04-03 | キナーゼ阻害剤としてのピラゾリル−ピリミジン誘導体 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US9284298B2 (enExample) |
| EP (1) | EP2702055A1 (enExample) |
| JP (1) | JP5976778B2 (enExample) |
| WO (1) | WO2012139930A1 (enExample) |
Families Citing this family (60)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR077468A1 (es) | 2009-07-09 | 2011-08-31 | Array Biopharma Inc | Compuestos de pirazolo (1,5 -a) pirimidina sustituidos como inhibidores de trk- quinasa |
| JO3215B1 (ar) | 2012-08-09 | 2018-03-08 | Phenex Pharmaceuticals Ag | حلقات غير متجانسة بها 5 ذرات تحتوي على النيتروجين بها استبدال بكربوكساميد أو سلفوناميد كمعدلات لمستقبل نووي غير محمي RORy |
| WO2014108337A1 (en) * | 2013-01-10 | 2014-07-17 | Grünenthal GmbH | Pyrazolyl-based carboxamides i as crac channel inhibitors |
| AU2014204977A1 (en) | 2013-01-10 | 2015-08-20 | Grunenthal Gmbh | Pyrazolyl-based carboxamides II as CRAC channel inhibitors |
| EP2943485B1 (en) | 2013-01-14 | 2017-09-20 | Incyte Holdings Corporation | Bicyclic aromatic carboxamide compounds useful as pim kinase inhibitors |
| HUE050215T2 (hu) | 2013-01-15 | 2020-11-30 | Incyte Holdings Corp | Pim kináz inhibitorokként hasznos tiazolkarboxamid és piridinkarboxamid vegyületek |
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- 2012-04-03 WO PCT/EP2012/056047 patent/WO2012139930A1/en not_active Ceased
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