JP2009539998A5 - - Google Patents
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- JP2009539998A5 JP2009539998A5 JP2009515487A JP2009515487A JP2009539998A5 JP 2009539998 A5 JP2009539998 A5 JP 2009539998A5 JP 2009515487 A JP2009515487 A JP 2009515487A JP 2009515487 A JP2009515487 A JP 2009515487A JP 2009539998 A5 JP2009539998 A5 JP 2009539998A5
- Authority
- JP
- Japan
- Prior art keywords
- indol
- nicotinonitrile
- methyl
- amino
- ylamino
- 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.)
- Withdrawn
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- -1 benzodioxanyl group Chemical group 0.000 claims description 398
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 192
- GZPHSAQLYPIAIN-UHFFFAOYSA-N 3-pyridinecarbonitrile Chemical compound N#CC1=CC=CN=C1 GZPHSAQLYPIAIN-UHFFFAOYSA-N 0.000 claims description 160
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 68
- 125000000217 alkyl group Chemical group 0.000 claims description 54
- 150000001875 compounds Chemical class 0.000 claims description 53
- 150000002148 esters Chemical class 0.000 claims description 48
- 150000003839 salts Chemical class 0.000 claims description 48
- 125000004195 4-methylpiperazin-1-yl group Chemical group [H]C([H])([H])N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims description 36
- 125000001072 heteroaryl group Chemical group 0.000 claims description 34
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 32
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 30
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 30
- 125000003118 aryl group Chemical group 0.000 claims description 29
- 125000001188 haloalkyl group Chemical group 0.000 claims description 28
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 24
- 125000003762 3,4-dimethoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 claims description 24
- 125000000304 alkynyl group Chemical group 0.000 claims description 22
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 22
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 14
- 229910052736 halogen Inorganic materials 0.000 claims description 14
- 150000002367 halogens Chemical class 0.000 claims description 14
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims description 12
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 12
- 125000003342 alkenyl group Chemical group 0.000 claims description 9
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 7
- LUQVCHRDAGWYMG-UHFFFAOYSA-N 4-phenylbenzamide Chemical compound C1=CC(C(=O)N)=CC=C1C1=CC=CC=C1 LUQVCHRDAGWYMG-UHFFFAOYSA-N 0.000 claims description 6
- 241000124008 Mammalia Species 0.000 claims description 6
- 102000001253 Protein Kinase Human genes 0.000 claims description 6
- 206010003246 arthritis Diseases 0.000 claims description 6
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims description 6
- 208000035475 disorder Diseases 0.000 claims description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
- 150000004677 hydrates Chemical class 0.000 claims description 6
- 125000001041 indolyl group Chemical group 0.000 claims description 6
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 6
- 108060006633 protein kinase Proteins 0.000 claims description 6
- 125000004076 pyridyl group Chemical group 0.000 claims description 6
- 125000000168 pyrrolyl group Chemical group 0.000 claims description 6
- 125000001544 thienyl group Chemical group 0.000 claims description 6
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims description 5
- 230000001575 pathological effect Effects 0.000 claims description 5
- 125000004484 1-methylpiperidin-4-yl group Chemical group CN1CCC(CC1)* 0.000 claims description 4
- 125000006012 2-chloroethoxy group Chemical group 0.000 claims description 4
- IMEYANPAYSSKRC-UHFFFAOYSA-N 4-[(4-methyl-1h-indol-5-yl)amino]-5-[4-(piperazin-1-ylmethyl)phenyl]pyridine-3-carbonitrile Chemical compound C1=CC=2NC=CC=2C(C)=C1NC1=C(C#N)C=NC=C1C(C=C1)=CC=C1CN1CCNCC1 IMEYANPAYSSKRC-UHFFFAOYSA-N 0.000 claims description 4
- 125000000928 benzodioxinyl group Chemical group O1C(=COC2=C1C=CC=C2)* 0.000 claims description 4
- 125000002047 benzodioxolyl group Chemical group O1OC(C2=C1C=CC=C2)* 0.000 claims description 4
- 239000003814 drug Substances 0.000 claims description 4
- 125000002541 furyl group Chemical group 0.000 claims description 4
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 claims description 4
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 claims description 4
- 125000004531 indol-5-yl group Chemical group [H]N1C([H])=C([H])C2=C([H])C(*)=C([H])C([H])=C12 0.000 claims description 4
- 230000001404 mediated effect Effects 0.000 claims description 4
- 125000002757 morpholinyl group Chemical group 0.000 claims description 4
- DXASQZJWWGZNSF-UHFFFAOYSA-N n,n-dimethylmethanamine;sulfur trioxide Chemical group CN(C)C.O=S(=O)=O DXASQZJWWGZNSF-UHFFFAOYSA-N 0.000 claims description 4
- 125000001624 naphthyl group Chemical group 0.000 claims description 4
- 125000004193 piperazinyl group Chemical group 0.000 claims description 4
- 125000003386 piperidinyl group Chemical group 0.000 claims description 4
- 125000003367 polycyclic group Chemical group 0.000 claims description 4
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 4
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 4
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 4
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims description 4
- 125000004568 thiomorpholinyl group Chemical group 0.000 claims description 4
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 3
- 125000006708 (C5-C14) heteroaryl group Chemical group 0.000 claims description 3
- 208000023275 Autoimmune disease Diseases 0.000 claims description 3
- 201000004681 Psoriasis Diseases 0.000 claims description 3
- 208000006673 asthma Diseases 0.000 claims description 3
- 206010009887 colitis Diseases 0.000 claims description 3
- 239000003937 drug carrier Substances 0.000 claims description 3
- 230000002401 inhibitory effect Effects 0.000 claims description 3
- 208000018937 joint inflammation Diseases 0.000 claims description 3
- 201000006417 multiple sclerosis Diseases 0.000 claims description 3
- 201000008482 osteoarthritis Diseases 0.000 claims description 3
- 239000008194 pharmaceutical composition Substances 0.000 claims description 3
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 3
- 206010039073 rheumatoid arthritis Diseases 0.000 claims description 3
- GJKWRHRABCZMIU-UHFFFAOYSA-N 1-[4-[5-cyano-4-[(4-methyl-1h-indol-5-yl)amino]pyridin-3-yl]phenyl]-3-cyclopropylurea Chemical compound C1=CC=2NC=CC=2C(C)=C1NC1=C(C#N)C=NC=C1C(C=C1)=CC=C1NC(=O)NC1CC1 GJKWRHRABCZMIU-UHFFFAOYSA-N 0.000 claims description 2
- KTOSRFZTOAPGSV-UHFFFAOYSA-N 1-[4-[5-cyano-4-[(4-methyl-1h-indol-5-yl)amino]pyridin-3-yl]phenyl]-3-methylurea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=CN=CC(C#N)=C1NC1=CC=C(NC=C2)C2=C1C KTOSRFZTOAPGSV-UHFFFAOYSA-N 0.000 claims description 2
- CKNLVXULMPJWNO-UHFFFAOYSA-N 1-butyl-3-[4-[5-cyano-4-[(4-methyl-1h-indol-5-yl)amino]pyridin-3-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NCCCC)=CC=C1C1=CN=CC(C#N)=C1NC1=CC=C(NC=C2)C2=C1C CKNLVXULMPJWNO-UHFFFAOYSA-N 0.000 claims description 2
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims description 2
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims description 2
- ZYHQGITXIJDDKC-UHFFFAOYSA-N 2-[2-(2-aminophenyl)ethyl]aniline Chemical group NC1=CC=CC=C1CCC1=CC=CC=C1N ZYHQGITXIJDDKC-UHFFFAOYSA-N 0.000 claims description 2
- HCRYHRHBOYXHAI-UHFFFAOYSA-N 2-[5-cyano-4-(1h-indol-4-ylamino)pyridin-3-yl]-n,n-dimethylbenzenesulfonamide Chemical compound CN(C)S(=O)(=O)C1=CC=CC=C1C1=CN=CC(C#N)=C1NC1=CC=CC2=C1C=CN2 HCRYHRHBOYXHAI-UHFFFAOYSA-N 0.000 claims description 2
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims description 2
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims description 2
- LJGHYPLBDBRCRZ-UHFFFAOYSA-N 3-(3-aminophenyl)sulfonylaniline Chemical group NC1=CC=CC(S(=O)(=O)C=2C=C(N)C=CC=2)=C1 LJGHYPLBDBRCRZ-UHFFFAOYSA-N 0.000 claims description 2
- KMWPZWCJOGJZFF-UHFFFAOYSA-N 3-[3-[5-cyano-4-(1h-indol-5-ylamino)pyridin-3-yl]phenyl]-n-cyclopentylbenzamide Chemical compound C=1C=CC(C=2C=C(C=CC=2)C=2C(=C(C#N)C=NC=2)NC=2C=C3C=CNC3=CC=2)=CC=1C(=O)NC1CCCC1 KMWPZWCJOGJZFF-UHFFFAOYSA-N 0.000 claims description 2
- GUNHRJLTFBDYOS-UHFFFAOYSA-N 3-[4-[5-cyano-4-[(4-methyl-1h-indol-5-yl)amino]pyridin-3-yl]phenyl]-1,1-dimethylurea Chemical compound C1=CC(NC(=O)N(C)C)=CC=C1C1=CN=CC(C#N)=C1NC1=CC=C(NC=C2)C2=C1C GUNHRJLTFBDYOS-UHFFFAOYSA-N 0.000 claims description 2
- QIXANBDZSYPCBY-UHFFFAOYSA-N 3-[5-cyano-4-(1h-indol-4-ylamino)pyridin-3-yl]-n,n-dimethylbenzamide Chemical compound CN(C)C(=O)C1=CC=CC(C=2C(=C(C#N)C=NC=2)NC=2C=3C=CNC=3C=CC=2)=C1 QIXANBDZSYPCBY-UHFFFAOYSA-N 0.000 claims description 2
- BKTWQXGKBHVHMZ-UHFFFAOYSA-N 3-[5-cyano-4-(1h-indol-4-ylamino)pyridin-3-yl]-n,n-dimethylbenzenesulfonamide Chemical compound CN(C)S(=O)(=O)C1=CC=CC(C=2C(=C(C#N)C=NC=2)NC=2C=3C=CNC=3C=CC=2)=C1 BKTWQXGKBHVHMZ-UHFFFAOYSA-N 0.000 claims description 2
- RCBIKUQGUQRBRL-UHFFFAOYSA-N 3-[5-cyano-4-(1h-indol-4-ylamino)pyridin-3-yl]benzamide Chemical compound NC(=O)C1=CC=CC(C=2C(=C(C#N)C=NC=2)NC=2C=3C=CNC=3C=CC=2)=C1 RCBIKUQGUQRBRL-UHFFFAOYSA-N 0.000 claims description 2
- NEZMRASZNJZDQH-UHFFFAOYSA-N 3-[5-cyano-4-(1h-indol-4-ylamino)pyridin-3-yl]benzoic acid Chemical compound OC(=O)C1=CC=CC(C=2C(=C(C#N)C=NC=2)NC=2C=3C=CNC=3C=CC=2)=C1 NEZMRASZNJZDQH-UHFFFAOYSA-N 0.000 claims description 2
- PDUJSKGQCLEINP-UHFFFAOYSA-N 3-[5-cyano-4-[(4-methyl-1h-indol-5-yl)amino]pyridin-3-yl]benzoic acid Chemical compound C1=CC=2NC=CC=2C(C)=C1NC1=C(C#N)C=NC=C1C1=CC=CC(C(O)=O)=C1 PDUJSKGQCLEINP-UHFFFAOYSA-N 0.000 claims description 2
- 125000006275 3-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C([H])C(*)=C1[H] 0.000 claims description 2
- 125000004208 3-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C([H])C(*)=C1[H] 0.000 claims description 2
- 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 claims description 2
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 claims description 2
- AYVCYBNEDAUCGX-UHFFFAOYSA-N 4-(1,3-benzodioxol-5-ylamino)-5-(3,4-dimethoxyphenyl)pyridine-3-carbonitrile Chemical compound C1=C(OC)C(OC)=CC=C1C1=CN=CC(C#N)=C1NC1=CC=C(OCO2)C2=C1 AYVCYBNEDAUCGX-UHFFFAOYSA-N 0.000 claims description 2
- MYRDYXMQEOXLRT-UHFFFAOYSA-N 4-(1,3-benzothiazol-6-ylamino)-5-[3-methoxy-4-(2-methoxyethoxy)phenyl]pyridine-3-carbonitrile Chemical compound C1=C(OC)C(OCCOC)=CC=C1C1=CN=CC(C#N)=C1NC1=CC=C(N=CS2)C2=C1 MYRDYXMQEOXLRT-UHFFFAOYSA-N 0.000 claims description 2
- BDTALRYKZNZRDD-UHFFFAOYSA-N 4-(1,3-benzothiazol-6-ylamino)-5-[4-methoxy-3-(2-methoxyethoxy)phenyl]pyridine-3-carbonitrile Chemical compound C1=C(OC)C(OCCOC)=CC(C=2C(=C(C#N)C=NC=2)NC=2C=C3SC=NC3=CC=2)=C1 BDTALRYKZNZRDD-UHFFFAOYSA-N 0.000 claims description 2
- KAECSRGNEJKWJC-UHFFFAOYSA-N 4-(1h-indazol-5-ylamino)-5-(3-methoxyphenyl)pyridine-3-carbonitrile Chemical compound COC1=CC=CC(C=2C(=C(C#N)C=NC=2)NC=2C=C3C=NNC3=CC=2)=C1 KAECSRGNEJKWJC-UHFFFAOYSA-N 0.000 claims description 2
- WEBWAJMEXBHJLH-UHFFFAOYSA-N 4-(1h-indazol-6-ylamino)-5-(3-methoxyphenyl)pyridine-3-carbonitrile Chemical compound COC1=CC=CC(C=2C(=C(C#N)C=NC=2)NC=2C=C3NN=CC3=CC=2)=C1 WEBWAJMEXBHJLH-UHFFFAOYSA-N 0.000 claims description 2
- WHBKXCTYGHTRJY-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-(2-methoxyphenyl)pyridine-3-carbonitrile Chemical compound COC1=CC=CC=C1C1=CN=CC(C#N)=C1NC1=CC=CC2=C1C=CN2 WHBKXCTYGHTRJY-UHFFFAOYSA-N 0.000 claims description 2
- ONBJHMOEYBCQIK-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-(3-methylsulfonylphenyl)pyridine-3-carbonitrile Chemical compound CS(=O)(=O)C1=CC=CC(C=2C(=C(C#N)C=NC=2)NC=2C=3C=CNC=3C=CC=2)=C1 ONBJHMOEYBCQIK-UHFFFAOYSA-N 0.000 claims description 2
- UNYSCSDWXYXDRM-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-(4-methoxyphenyl)pyridine-3-carbonitrile Chemical compound C1=CC(OC)=CC=C1C1=CN=CC(C#N)=C1NC1=CC=CC2=C1C=CN2 UNYSCSDWXYXDRM-UHFFFAOYSA-N 0.000 claims description 2
- VFNLQYOUKPRALX-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-[1-(4-methylphenyl)sulfonylindol-3-yl]pyridine-3-carbonitrile Chemical compound C1=CC(C)=CC=C1S(=O)(=O)N1C2=CC=CC=C2C(C=2C(=C(C#N)C=NC=2)NC=2C=3C=CNC=3C=CC=2)=C1 VFNLQYOUKPRALX-UHFFFAOYSA-N 0.000 claims description 2
- OVMXFSZIFQUQRH-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-[3-(2-methoxyethoxy)phenyl]pyridine-3-carbonitrile Chemical compound COCCOC1=CC=CC(C=2C(=C(C#N)C=NC=2)NC=2C=3C=CNC=3C=CC=2)=C1 OVMXFSZIFQUQRH-UHFFFAOYSA-N 0.000 claims description 2
- QEKLUEUSIGZNIT-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-[3-(2-morpholin-4-ylethoxy)phenyl]pyridine-3-carbonitrile Chemical compound C=1C=CC=2NC=CC=2C=1NC=1C(C#N)=CN=CC=1C(C=1)=CC=CC=1OCCN1CCOCC1 QEKLUEUSIGZNIT-UHFFFAOYSA-N 0.000 claims description 2
- WMEKLMVCWRPPGA-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-[3-(2-piperidin-1-ylethoxy)phenyl]pyridine-3-carbonitrile Chemical compound C=1C=CC=2NC=CC=2C=1NC=1C(C#N)=CN=CC=1C(C=1)=CC=CC=1OCCN1CCCCC1 WMEKLMVCWRPPGA-UHFFFAOYSA-N 0.000 claims description 2
- CDSMVYVAOJOBOE-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-[3-(2-pyrrolidin-1-ylethoxy)phenyl]pyridine-3-carbonitrile Chemical compound C=1C=CC=2NC=CC=2C=1NC=1C(C#N)=CN=CC=1C(C=1)=CC=CC=1OCCN1CCCC1 CDSMVYVAOJOBOE-UHFFFAOYSA-N 0.000 claims description 2
- MMVHNEPFDQHBTM-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-[3-[2-(4-methylpiperazin-1-yl)ethoxy]phenyl]pyridine-3-carbonitrile Chemical compound C1CN(C)CCN1CCOC1=CC=CC(C=2C(=C(C#N)C=NC=2)NC=2C=3C=CNC=3C=CC=2)=C1 MMVHNEPFDQHBTM-UHFFFAOYSA-N 0.000 claims description 2
- NCPMIPMGHYJCNG-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-[3-[4-(pyrrolidine-1-carbonyl)phenyl]phenyl]pyridine-3-carbonitrile Chemical compound C=1C=C(C=2C=C(C=CC=2)C=2C(=C(C#N)C=NC=2)NC=2C=3C=CNC=3C=CC=2)C=CC=1C(=O)N1CCCC1 NCPMIPMGHYJCNG-UHFFFAOYSA-N 0.000 claims description 2
- IWRCRIJOOGSJGK-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-[3-methoxy-4-(2-methoxyethoxy)phenyl]pyridine-3-carbonitrile Chemical compound C1=C(OC)C(OCCOC)=CC=C1C1=CN=CC(C#N)=C1NC1=CC=CC2=C1C=CN2 IWRCRIJOOGSJGK-UHFFFAOYSA-N 0.000 claims description 2
- NYYMOTTUMJLICS-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-[4-(2-morpholin-4-ylethoxy)phenyl]pyridine-3-carbonitrile Chemical compound C=1C=CC=2NC=CC=2C=1NC=1C(C#N)=CN=CC=1C(C=C1)=CC=C1OCCN1CCOCC1 NYYMOTTUMJLICS-UHFFFAOYSA-N 0.000 claims description 2
- ZPKBYERIJJCKAI-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-[4-[2-(4-methylpiperazin-1-yl)ethoxy]phenyl]pyridine-3-carbonitrile Chemical compound C1CN(C)CCN1CCOC1=CC=C(C=2C(=C(C#N)C=NC=2)NC=2C=3C=CNC=3C=CC=2)C=C1 ZPKBYERIJJCKAI-UHFFFAOYSA-N 0.000 claims description 2
- OQGXWJUPOQZCMP-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-[4-methoxy-3-(2-methoxyethoxy)phenyl]pyridine-3-carbonitrile Chemical compound C1=C(OC)C(OCCOC)=CC(C=2C(=C(C#N)C=NC=2)NC=2C=3C=CNC=3C=CC=2)=C1 OQGXWJUPOQZCMP-UHFFFAOYSA-N 0.000 claims description 2
- SMSCTXBNQPWSJB-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-[4-methoxy-3-(2-morpholin-4-ylethoxy)phenyl]pyridine-3-carbonitrile Chemical compound COC1=CC=C(C=2C(=C(C#N)C=NC=2)NC=2C=3C=CNC=3C=CC=2)C=C1OCCN1CCOCC1 SMSCTXBNQPWSJB-UHFFFAOYSA-N 0.000 claims description 2
- DLEATKJPWWNGHU-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-[4-methoxy-3-(2-piperidin-1-ylethoxy)phenyl]pyridine-3-carbonitrile Chemical compound COC1=CC=C(C=2C(=C(C#N)C=NC=2)NC=2C=3C=CNC=3C=CC=2)C=C1OCCN1CCCCC1 DLEATKJPWWNGHU-UHFFFAOYSA-N 0.000 claims description 2
- UMYMVHQYASZFES-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-[4-methoxy-3-[2-(3-phenylpropylamino)ethoxy]phenyl]pyridine-3-carbonitrile Chemical compound COC1=CC=C(C=2C(=C(C#N)C=NC=2)NC=2C=3C=CNC=3C=CC=2)C=C1OCCNCCCC1=CC=CC=C1 UMYMVHQYASZFES-UHFFFAOYSA-N 0.000 claims description 2
- DQUUANKBPSGREK-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-[4-methoxy-3-[2-(3-pyrrolidin-1-ylpropylamino)ethoxy]phenyl]pyridine-3-carbonitrile Chemical compound COC1=CC=C(C=2C(=C(C#N)C=NC=2)NC=2C=3C=CNC=3C=CC=2)C=C1OCCNCCCN1CCCC1 DQUUANKBPSGREK-UHFFFAOYSA-N 0.000 claims description 2
- KRALBDOCPZMWIS-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-[4-methoxy-3-[2-(4-methylpiperazin-1-yl)ethoxy]phenyl]pyridine-3-carbonitrile Chemical compound COC1=CC=C(C=2C(=C(C#N)C=NC=2)NC=2C=3C=CNC=3C=CC=2)C=C1OCCN1CCN(C)CC1 KRALBDOCPZMWIS-UHFFFAOYSA-N 0.000 claims description 2
- FMHLBNDERLRCDO-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-[4-methoxy-3-[2-[2-(1-methylpyrrolidin-2-yl)ethylamino]ethoxy]phenyl]pyridine-3-carbonitrile Chemical compound COC1=CC=C(C=2C(=C(C#N)C=NC=2)NC=2C=3C=CNC=3C=CC=2)C=C1OCCNCCC1CCCN1C FMHLBNDERLRCDO-UHFFFAOYSA-N 0.000 claims description 2
- VYKNGSAUNAORNC-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-[4-methoxy-3-[2-[3-(2-oxopyrrolidin-1-yl)propylamino]ethoxy]phenyl]pyridine-3-carbonitrile Chemical compound COC1=CC=C(C=2C(=C(C#N)C=NC=2)NC=2C=3C=CNC=3C=CC=2)C=C1OCCNCCCN1CCCC1=O VYKNGSAUNAORNC-UHFFFAOYSA-N 0.000 claims description 2
- JBQXWZHNCFEWOV-UHFFFAOYSA-N 4-(1h-indol-4-ylamino)-5-[5-(morpholin-4-ylmethyl)-1-benzothiophen-2-yl]pyridine-3-carbonitrile Chemical compound C=1C=CC=2NC=CC=2C=1NC=1C(C#N)=CN=CC=1C(SC1=CC=2)=CC1=CC=2CN1CCOCC1 JBQXWZHNCFEWOV-UHFFFAOYSA-N 0.000 claims description 2
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- 125000004404 heteroalkyl group Chemical group 0.000 claims 9
- 239000000203 mixture Substances 0.000 claims 3
- JWZZKOKVBUJMES-UHFFFAOYSA-N (+-)-Isoprenaline Chemical compound CC(C)NCC(O)C1=CC=C(O)C(O)=C1 JWZZKOKVBUJMES-UHFFFAOYSA-N 0.000 claims 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 230000002757 inflammatory effect Effects 0.000 claims 1
- 125000004173 1-benzimidazolyl group Chemical group [H]C1=NC2=C([H])C([H])=C([H])C([H])=C2N1* 0.000 description 1
- 208000037979 autoimmune inflammatory disease Diseases 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 125000001977 isobenzofuranyl group Chemical group C=1(OC=C2C=CC=CC12)* 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US81306006P | 2006-06-13 | 2006-06-13 | |
| PCT/US2007/013954 WO2007146376A2 (en) | 2006-06-13 | 2007-06-13 | Substituted 3-cyanopyridines as protein kinase inhibitors |
Publications (2)
| Publication Number | Publication Date |
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| JP2009539998A JP2009539998A (ja) | 2009-11-19 |
| JP2009539998A5 true JP2009539998A5 (cg-RX-API-DMAC7.html) | 2010-07-29 |
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| JP2009515487A Withdrawn JP2009539998A (ja) | 2006-06-13 | 2007-06-13 | プロテインキナーゼ阻害剤としての置換3−シアノピリジン |
Country Status (18)
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2027093A2 (en) * | 2006-06-13 | 2009-02-25 | Wyeth | Substituted cyanopyridines as protein kinase inhibitors |
| BRPI0918846A2 (pt) * | 2008-09-02 | 2019-09-24 | Novartis Ag | inibidores de cinase heterocíclica |
| CN113735785B (zh) * | 2020-05-28 | 2023-10-13 | 南京桦冠生物技术有限公司 | 3,6-二氯吡嗪-2-甲腈的制备方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE255575T1 (de) * | 1998-09-29 | 2003-12-15 | Wyeth Corp | Substituierte 3-cyanochinoline als protein tyrosine kinase inhibitoren |
| AR037438A1 (es) * | 2001-11-27 | 2004-11-10 | Wyeth Corp | 3-cianoquinolinas como inhibidores de egf-r y her2 quinasas, un proceso para su preparacion, composiciones farmaceuticas y el uso de dichos compuestos para la fabricacion de medicamentos |
| MXPA05006367A (es) * | 2002-12-12 | 2005-08-29 | Pharmacia Corp | Metodo de uso de compuestos de aminocianopiridina como inhibidores de cinasa-2 de proteina activada de cinasa de proteina activada por mitogeno. |
| EP1888529A2 (en) * | 2005-05-18 | 2008-02-20 | Wyeth | 3-cyanoquinoline inhibitors of tpl2 kinase and methods of making and using the same |
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2007
- 2007-06-13 RU RU2008139079/04A patent/RU2008139079A/ru not_active Application Discontinuation
- 2007-06-13 JP JP2009515487A patent/JP2009539998A/ja not_active Withdrawn
- 2007-06-13 EP EP07796104.3A patent/EP2029543B1/en not_active Not-in-force
- 2007-06-13 KR KR1020087028580A patent/KR20090018612A/ko not_active Withdrawn
- 2007-06-13 MX MX2008015802A patent/MX2008015802A/es active IP Right Grant
- 2007-06-13 WO PCT/US2007/013954 patent/WO2007146376A2/en not_active Ceased
- 2007-06-13 AR ARP070102593A patent/AR061368A1/es unknown
- 2007-06-13 TW TW096121311A patent/TW200815407A/zh unknown
- 2007-06-13 ES ES07796104T patent/ES2558706T3/es active Active
- 2007-06-13 CN CN2007800216875A patent/CN101466678B/zh not_active Expired - Fee Related
- 2007-06-13 BR BRPI0712737-5A patent/BRPI0712737A2/pt not_active IP Right Cessation
- 2007-06-13 PE PE2007000746A patent/PE20080336A1/es not_active Application Discontinuation
- 2007-06-13 CL CL2007001737A patent/CL2007001737A1/es unknown
- 2007-06-13 CA CA2654515A patent/CA2654515C/en not_active Expired - Fee Related
- 2007-06-13 AU AU2007258237A patent/AU2007258237A1/en not_active Abandoned
-
2008
- 2008-10-07 IL IL194625A patent/IL194625A0/en unknown
- 2008-11-10 NO NO20084739A patent/NO20084739L/no not_active Application Discontinuation
- 2008-12-12 ZA ZA200810573A patent/ZA200810573B/xx unknown
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