JP2013507449A5

JP2013507449A5 -

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Publication number: JP2013507449A5
Authority: JP; Japan
Prior art keywords: amino; pyrimidin; phenyl; yloxy; pyran
Prior art date: 2010-10-12
Legal status : Pending

Application number

JP2012534299A

Other languages

English (en)

Japanese (ja)

Other versions

JP2013507449A (ja

Filing date

2010-10-12

Publication date

2013-11-28

2010-10-12 Application filed filed Critical

2010-10-12 Priority claimed from PCT/US2010/052385 external-priority patent/WO2011046970A1/en

2013-03-04 Publication of JP2013507449A publication Critical patent/JP2013507449A/ja

2013-11-28 Publication of JP2013507449A5 publication Critical patent/JP2013507449A5/ja

Status Pending legal-status Critical Current

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150000001875 compounds Chemical class 0.000 claims description 114
239000000203 mixture Substances 0.000 claims description 91
125000000217 alkyl group Chemical group 0.000 claims description 87
125000000623 heterocyclic group Chemical group 0.000 claims description 79
-1 carbocycle Chemical group 0.000 claims description 71
150000003839 salts Chemical class 0.000 claims description 55
125000001424 substituent group Chemical group 0.000 claims description 55
125000003545 alkoxy group Chemical group 0.000 claims description 36
125000001072 heteroaryl group Chemical group 0.000 claims description 34
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 34
208000001072 type 2 diabetes mellitus Diseases 0.000 claims description 34
125000000753 cycloalkyl group Chemical group 0.000 claims description 28
125000001145 hydrido group Chemical group *[H] 0.000 claims description 28
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 27
ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 claims description 25
125000005843 halogen group Chemical group 0.000 claims description 23
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 23
230000002159 abnormal effect Effects 0.000 claims description 21
238000009825 accumulation Methods 0.000 claims description 21
206010025135 lupus erythematosus Diseases 0.000 claims description 21
125000003118 aryl group Chemical group 0.000 claims description 20
230000001086 cytosolic effect Effects 0.000 claims description 20
125000004103 aminoalkyl group Chemical group 0.000 claims description 19
201000002481 Myositis Diseases 0.000 claims description 18
208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims description 17
208000015872 Gaucher disease Diseases 0.000 claims description 17
208000022559 Inflammatory bowel disease Diseases 0.000 claims description 17
206010022489 Insulin Resistance Diseases 0.000 claims description 17
208000001145 Metabolic Syndrome Diseases 0.000 claims description 17
206010028980 Neoplasm Diseases 0.000 claims description 17
208000008589 Obesity Diseases 0.000 claims description 17
201000004681 Psoriasis Diseases 0.000 claims description 17
208000021386 Sjogren Syndrome Diseases 0.000 claims description 17
201000000690 abdominal obesity-metabolic syndrome Diseases 0.000 claims description 17
201000011510 cancer Diseases 0.000 claims description 17
208000002551 irritable bowel syndrome Diseases 0.000 claims description 17
235000020824 obesity Nutrition 0.000 claims description 17
208000005987 polymyositis Diseases 0.000 claims description 17
208000019745 retinal vasculopathy with cerebral leukodystrophy Diseases 0.000 claims description 17
208000029941 retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations Diseases 0.000 claims description 17
208000001034 Frostbite Diseases 0.000 claims description 16
206010061218 Inflammation Diseases 0.000 claims description 16
201000001981 dermatomyositis Diseases 0.000 claims description 16
125000001188 haloalkyl group Chemical group 0.000 claims description 16
230000004054 inflammatory process Effects 0.000 claims description 16
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 15
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 15
239000003814 drug Substances 0.000 claims description 15
239000008194 pharmaceutical composition Substances 0.000 claims description 15
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 15
201000010099 disease Diseases 0.000 claims description 14
201000009594 Systemic Scleroderma Diseases 0.000 claims description 13
206010042953 Systemic sclerosis Diseases 0.000 claims description 13
JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims description 13
150000007523 nucleic acids Chemical class 0.000 claims description 13
102000039446 nucleic acids Human genes 0.000 claims description 13
108020004707 nucleic acids Proteins 0.000 claims description 13
125000002102 aryl alkyloxo group Chemical group 0.000 claims description 12
208000037765 diseases and disorders Diseases 0.000 claims description 12
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 12
125000000547 substituted alkyl group Chemical group 0.000 claims description 12
150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 10
125000005114 heteroarylalkoxy group Chemical group 0.000 claims description 10
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 9
125000004414 alkyl thio group Chemical group 0.000 claims description 9
150000001408 amides Chemical class 0.000 claims description 9
125000001589 carboacyl group Chemical group 0.000 claims description 9
125000005366 cycloalkylthio group Chemical group 0.000 claims description 9
125000003396 thiol group Chemical class [H]S* 0.000 claims description 9
101000665442 Homo sapiens Serine/threonine-protein kinase TBK1 Proteins 0.000 claims description 8
102100038192 Serine/threonine-protein kinase TBK1 Human genes 0.000 claims description 8
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 8
230000000694 effects Effects 0.000 claims description 8
125000004446 heteroarylalkyl group Chemical group 0.000 claims description 8
125000005553 heteroaryloxy group Chemical group 0.000 claims description 8
238000002560 therapeutic procedure Methods 0.000 claims description 8
102000001284 I-kappa-B kinase Human genes 0.000 claims description 7
108060006678 I-kappa-B kinase Proteins 0.000 claims description 7
108091000080 Phosphotransferase Proteins 0.000 claims description 7
125000003710 aryl alkyl group Chemical group 0.000 claims description 7
229910052799 carbon Inorganic materials 0.000 claims description 7
125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims description 7
125000004470 heterocyclooxy group Chemical group 0.000 claims description 7
102000020233 phosphotransferase Human genes 0.000 claims description 7
125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 claims description 7
SXNKDLAJDADKEE-UHFFFAOYSA-N 2-(oxan-4-yloxy)benzonitrile Chemical compound N#CC1=CC=CC=C1OC1CCOCC1 SXNKDLAJDADKEE-UHFFFAOYSA-N 0.000 claims description 6
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 6
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 6
125000003282 alkyl amino group Chemical group 0.000 claims description 5
125000003277 amino group Chemical group 0.000 claims description 5
230000002401 inhibitory effect Effects 0.000 claims description 5
125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 claims description 5
208000024891 symptom Diseases 0.000 claims description 5
YRZGLSVFCMYTOI-UHFFFAOYSA-N 2-carboxyoxy-2-oxoacetic acid Chemical compound OC(=O)OC(=O)C(O)=O YRZGLSVFCMYTOI-UHFFFAOYSA-N 0.000 claims description 4
GBHLNZCFYHLBJP-UHFFFAOYSA-N 2-hydroxy-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C1=C(C#N)C(O)=CC=C1C1=CC=NC(NC=2C=CC(=CC=2)N2CCOCC2)=N1 GBHLNZCFYHLBJP-UHFFFAOYSA-N 0.000 claims description 4
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 4
KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims description 4
208000034189 Sclerosis Diseases 0.000 claims description 4
125000003342 alkenyl group Chemical group 0.000 claims description 4
125000004450 alkenylene group Chemical group 0.000 claims description 4
125000005083 alkoxyalkoxy group Chemical group 0.000 claims description 4
125000002947 alkylene group Chemical group 0.000 claims description 4
125000000304 alkynyl group Chemical group 0.000 claims description 4
125000005133 alkynyloxy group Chemical group 0.000 claims description 4
125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 claims description 4
125000005015 aryl alkynyl group Chemical group 0.000 claims description 4
125000005110 aryl thio group Chemical group 0.000 claims description 4
125000004104 aryloxy group Chemical group 0.000 claims description 4
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 4
125000005111 carboxyalkoxy group Chemical group 0.000 claims description 4
125000004181 carboxyalkyl group Chemical group 0.000 claims description 4
125000004093 cyano group Chemical group *C#N 0.000 claims description 4
125000000392 cycloalkenyl group Chemical group 0.000 claims description 4
125000000000 cycloalkoxy group Chemical group 0.000 claims description 4
150000002148 esters Chemical class 0.000 claims description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
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125000005842 heteroatom Chemical group 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 4
150000002825 nitriles Chemical class 0.000 claims description 4
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 claims description 4
HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 claims description 3
210000004027 cell Anatomy 0.000 claims description 3
125000005647 linker group Chemical group 0.000 claims description 3
150000004702 methyl esters Chemical class 0.000 claims description 3
125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 claims description 3
ZFAHEZVRPNTURF-MRXNPFEDSA-N (2r)-n-[3-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]phenyl]-2-hydroxypropanamide Chemical compound C[C@@H](O)C(=O)NC1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 ZFAHEZVRPNTURF-MRXNPFEDSA-N 0.000 claims description 2
LGWLOJATUSPIGW-LBAQZLPGSA-N (2s)-n-[2-cyano-4-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]phenyl]-2-fluorocyclopropane-1-carboxamide Chemical compound F[C@H]1CC1C(=O)NC1=CC=C(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)C=C1C#N LGWLOJATUSPIGW-LBAQZLPGSA-N 0.000 claims description 2
GRFWMCQLFKGLRL-KRWDZBQOSA-N (2s)-n-[[4-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]phenyl]methyl]-2-hydroxypropanamide Chemical compound C1=CC(CNC(=O)[C@@H](O)C)=CC=C1NC1=NC=CC(C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=N1 GRFWMCQLFKGLRL-KRWDZBQOSA-N 0.000 claims description 2
RXYZSERXOLXHOS-UHFFFAOYSA-N 1-[3-[[4-[3-cyano-4-(2-methylpropoxy)phenyl]pyrimidin-2-yl]amino]phenyl]-n-(2-hydroxyethyl)methanesulfonamide Chemical compound C1=C(C#N)C(OCC(C)C)=CC=C1C1=CC=NC(NC=2C=C(CS(=O)(=O)NCCO)C=CC=2)=N1 RXYZSERXOLXHOS-UHFFFAOYSA-N 0.000 claims description 2
SDCYGVQTXRDWPA-UHFFFAOYSA-N 1-[3-[[4-[3-cyano-4-(cyclopropylmethoxy)phenyl]pyrimidin-2-yl]amino]phenyl]-n-(2-hydroxyethyl)methanesulfonamide Chemical compound OCCNS(=O)(=O)CC1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(OCC3CC3)=CC=2)C#N)=C1 SDCYGVQTXRDWPA-UHFFFAOYSA-N 0.000 claims description 2
ZAZCZFWYSFVROW-UHFFFAOYSA-N 1-[3-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]phenyl]-3-(2-hydroxy-2-methylpropyl)urea Chemical compound CC(C)(O)CNC(=O)NC1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 ZAZCZFWYSFVROW-UHFFFAOYSA-N 0.000 claims description 2
SWQRGFVLXPGOJH-UHFFFAOYSA-N 1-[3-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]phenyl]-3-(2-hydroxyethyl)urea Chemical compound OCCNC(=O)NC1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 SWQRGFVLXPGOJH-UHFFFAOYSA-N 0.000 claims description 2
YDARQBPTAYZTPL-UHFFFAOYSA-N 1-[3-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]phenyl]-3-(2-methoxyethyl)urea Chemical compound COCCNC(=O)NC1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 YDARQBPTAYZTPL-UHFFFAOYSA-N 0.000 claims description 2
FWNAYSLSBKBCDS-UHFFFAOYSA-N 1-[3-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]phenyl]-3-(4-hydroxycyclohexyl)urea Chemical compound C1CC(O)CCC1NC(=O)NC1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 FWNAYSLSBKBCDS-UHFFFAOYSA-N 0.000 claims description 2
UOXHEKDPBOYOQK-UHFFFAOYSA-N 1-[3-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]phenyl]-n,n-dimethylmethanesulfonamide Chemical compound CN(C)S(=O)(=O)CC1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 UOXHEKDPBOYOQK-UHFFFAOYSA-N 0.000 claims description 2
MUMUPQIUNAYAOG-UHFFFAOYSA-N 1-[3-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]phenyl]-n-methylmethanesulfonamide Chemical compound CNS(=O)(=O)CC1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 MUMUPQIUNAYAOG-UHFFFAOYSA-N 0.000 claims description 2
WSSFUDAHEBFMGA-UHFFFAOYSA-N 1-[4-[[4-[3-cyano-4-(2-methylpropoxy)phenyl]pyrimidin-2-yl]amino]phenyl]-n-(2-hydroxyethyl)methanesulfonamide Chemical compound C1=C(C#N)C(OCC(C)C)=CC=C1C1=CC=NC(NC=2C=CC(CS(=O)(=O)NCCO)=CC=2)=N1 WSSFUDAHEBFMGA-UHFFFAOYSA-N 0.000 claims description 2
QXCSRCRWTXTNGV-UHFFFAOYSA-N 1-[4-[[4-[3-cyano-4-(2-methylpropoxy)phenyl]pyrimidin-2-yl]amino]phenyl]-n-methylmethanesulfonamide Chemical compound C1=CC(CS(=O)(=O)NC)=CC=C1NC1=NC=CC(C=2C=C(C(OCC(C)C)=CC=2)C#N)=N1 QXCSRCRWTXTNGV-UHFFFAOYSA-N 0.000 claims description 2
VCNTWDBWHXXDKV-UHFFFAOYSA-N 1-[4-[[4-[3-cyano-4-(cyclopropylmethoxy)phenyl]pyrimidin-2-yl]amino]phenyl]-n-(2-hydroxyethyl)methanesulfonamide Chemical compound C1=CC(CS(=O)(=O)NCCO)=CC=C1NC1=NC=CC(C=2C=C(C(OCC3CC3)=CC=2)C#N)=N1 VCNTWDBWHXXDKV-UHFFFAOYSA-N 0.000 claims description 2
AHQAVCZGZZIKNC-UHFFFAOYSA-N 1-[4-[[4-[3-cyano-4-(cyclopropylmethoxy)phenyl]pyrimidin-2-yl]amino]phenyl]-n-methylmethanesulfonamide Chemical compound C1=CC(CS(=O)(=O)NC)=CC=C1NC1=NC=CC(C=2C=C(C(OCC3CC3)=CC=2)C#N)=N1 AHQAVCZGZZIKNC-UHFFFAOYSA-N 0.000 claims description 2
BCSNTRDXBSJQKG-UHFFFAOYSA-N 1-[4-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]phenyl]-3-(2-hydroxyethyl)urea Chemical compound C1=CC(NC(=O)NCCO)=CC=C1NC1=NC=CC(C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=N1 BCSNTRDXBSJQKG-UHFFFAOYSA-N 0.000 claims description 2
BFBJJGCOPRQDRT-UHFFFAOYSA-N 1-[4-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]phenyl]-3-pyridin-3-ylurea Chemical compound C=1C=CN=CC=1NC(=O)NC(C=C1)=CC=C1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 BFBJJGCOPRQDRT-UHFFFAOYSA-N 0.000 claims description 2
DBANDVJDACQECW-UHFFFAOYSA-N 1-[4-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]phenyl]-n,n-dimethylmethanesulfonamide Chemical compound C1=CC(CS(=O)(=O)N(C)C)=CC=C1NC1=NC=CC(C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=N1 DBANDVJDACQECW-UHFFFAOYSA-N 0.000 claims description 2
ALPBKBJVWFGPCC-UHFFFAOYSA-N 1-[4-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]phenyl]-n-methylmethanesulfonamide Chemical compound C1=CC(CS(=O)(=O)NC)=CC=C1NC1=NC=CC(C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=N1 ALPBKBJVWFGPCC-UHFFFAOYSA-N 0.000 claims description 2
125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 2
YOMMJAVDVHKMEW-UHFFFAOYSA-N 2-(1-acetylpiperidin-4-yl)oxy-5-[2-(3,4,5-trimethoxyanilino)pyrimidin-4-yl]benzonitrile Chemical compound COC1=C(OC)C(OC)=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCN(CC3)C(C)=O)=CC=2)C#N)=C1 YOMMJAVDVHKMEW-UHFFFAOYSA-N 0.000 claims description 2
IJYNRMLUPGZUDQ-UHFFFAOYSA-N 2-(1-acetylpiperidin-4-yl)oxy-5-[2-[3-methoxy-4-(3-oxopiperazin-1-yl)anilino]pyrimidin-4-yl]benzonitrile Chemical compound C=1C=C(N2CC(=O)NCC2)C(OC)=CC=1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCN(C(C)=O)CC1 IJYNRMLUPGZUDQ-UHFFFAOYSA-N 0.000 claims description 2
RRFIOKKCKJOCGT-UHFFFAOYSA-N 2-(1-formylpiperidin-4-yl)oxy-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C1CN(C=O)CCC1OC1=CC=C(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)C=C1C#N RRFIOKKCKJOCGT-UHFFFAOYSA-N 0.000 claims description 2
HZYLZYIYBBZCST-UHFFFAOYSA-N 2-(1-methylsulfonylpiperidin-4-yl)oxy-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C1CN(S(=O)(=O)C)CCC1OC1=CC=C(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)C=C1C#N HZYLZYIYBBZCST-UHFFFAOYSA-N 0.000 claims description 2
WESICWARAPSFFU-UHFFFAOYSA-N 2-(2-hydroxy-2-methylpropoxy)-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C1=C(C#N)C(OCC(C)(O)C)=CC=C1C1=CC=NC(NC=2C=CC(=CC=2)N2CCOCC2)=N1 WESICWARAPSFFU-UHFFFAOYSA-N 0.000 claims description 2
DTVCHEBAZFOKGH-UHFFFAOYSA-N 2-(2-hydroxyethoxy)-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C1=C(C#N)C(OCCO)=CC=C1C1=CC=NC(NC=2C=CC(=CC=2)N2CCOCC2)=N1 DTVCHEBAZFOKGH-UHFFFAOYSA-N 0.000 claims description 2
WETHTRHZLRLMRV-UHFFFAOYSA-N 2-(2-methylpropoxy)-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C1=C(C#N)C(OCC(C)C)=CC=C1C1=CC=NC(NC=2C=CC(=CC=2)N2CCOCC2)=N1 WETHTRHZLRLMRV-UHFFFAOYSA-N 0.000 claims description 2
HWEQRUOYRCLLHQ-UHFFFAOYSA-N 2-(3-hydroxypropoxy)-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C1=C(C#N)C(OCCCO)=CC=C1C1=CC=NC(NC=2C=CC(=CC=2)N2CCOCC2)=N1 HWEQRUOYRCLLHQ-UHFFFAOYSA-N 0.000 claims description 2
ADIZNFICJNWZBL-UHFFFAOYSA-N 2-(cyclopropylmethoxy)-5-[2-(4-fluoro-3-pyrrolidin-3-yloxyanilino)pyrimidin-4-yl]benzonitrile Chemical compound C1=C(OC2CNCC2)C(F)=CC=C1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OCC1CC1 ADIZNFICJNWZBL-UHFFFAOYSA-N 0.000 claims description 2
QTYKNNVICQVSCR-UHFFFAOYSA-N 2-(cyclopropylmethoxy)-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)=CC=C1OCC1CC1 QTYKNNVICQVSCR-UHFFFAOYSA-N 0.000 claims description 2
ATULWOQVMPDHEO-UHFFFAOYSA-N 2-(cyclopropylmethoxy)-5-[2-[3-[2-(diethylamino)ethoxy]-4-fluoroanilino]pyrimidin-4-yl]benzonitrile Chemical compound C1=C(F)C(OCCN(CC)CC)=CC(NC=2N=C(C=CN=2)C=2C=C(C(OCC3CC3)=CC=2)C#N)=C1 ATULWOQVMPDHEO-UHFFFAOYSA-N 0.000 claims description 2
QFJYVSADODZKTH-UHFFFAOYSA-N 2-(cyclopropylmethoxy)-5-[2-[3-methoxy-4-(3-methoxyazetidine-1-carbonyl)anilino]pyrimidin-4-yl]benzonitrile Chemical compound C1C(OC)CN1C(=O)C(C(=C1)OC)=CC=C1NC1=NC=CC(C=2C=C(C(OCC3CC3)=CC=2)C#N)=N1 QFJYVSADODZKTH-UHFFFAOYSA-N 0.000 claims description 2
GNBHTMOOEQONAB-UHFFFAOYSA-N 2-(cyclopropylmethoxy)-5-[2-[3-methoxy-4-[(3-methoxyazetidin-1-yl)methyl]anilino]pyrimidin-4-yl]benzonitrile Chemical compound C1C(OC)CN1CC(C(=C1)OC)=CC=C1NC1=NC=CC(C=2C=C(C(OCC3CC3)=CC=2)C#N)=N1 GNBHTMOOEQONAB-UHFFFAOYSA-N 0.000 claims description 2
FGLZJVGRQXBRPF-UHFFFAOYSA-N 2-(cyclopropylmethoxy)-5-[2-[4-[(2-methoxyethylamino)methyl]anilino]pyrimidin-4-yl]benzonitrile Chemical compound C1=CC(CNCCOC)=CC=C1NC1=NC=CC(C=2C=C(C(OCC3CC3)=CC=2)C#N)=N1 FGLZJVGRQXBRPF-UHFFFAOYSA-N 0.000 claims description 2
LGOCEQKGULDJAT-UHFFFAOYSA-N 2-(cyclopropylmethoxy)-5-[2-[4-[4-(2-hydroxyethyl)piperazin-1-yl]anilino]pyrimidin-4-yl]benzonitrile Chemical compound C1CN(CCO)CCN1C(C=C1)=CC=C1NC1=NC=CC(C=2C=C(C(OCC3CC3)=CC=2)C#N)=N1 LGOCEQKGULDJAT-UHFFFAOYSA-N 0.000 claims description 2
QKYXVICVBJGDJG-UHFFFAOYSA-N 2-(cyclopropylmethoxy)-5-[2-[4-fluoro-3-(2-piperazin-1-ylethoxy)anilino]pyrimidin-4-yl]benzonitrile Chemical compound C1=C(OCCN2CCNCC2)C(F)=CC=C1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OCC1CC1 QKYXVICVBJGDJG-UHFFFAOYSA-N 0.000 claims description 2
BFBMZIOQTYVFRH-UHFFFAOYSA-N 2-(oxan-4-yloxy)-5-[2-(3,4,5-trimethoxyanilino)pyrimidin-4-yl]benzonitrile Chemical compound COC1=C(OC)C(OC)=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 BFBMZIOQTYVFRH-UHFFFAOYSA-N 0.000 claims description 2
QKGUAOLTNXDXIU-UHFFFAOYSA-N 2-(oxan-4-yloxy)-5-[2-(3-pyrazol-1-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=C(C=CC=3)N3N=CC=C3)N=CC=2)=CC=C1OC1CCOCC1 QKGUAOLTNXDXIU-UHFFFAOYSA-N 0.000 claims description 2
CZFNMENEUSTMAC-UHFFFAOYSA-N 2-(oxan-4-yloxy)-5-[2-(3-pyridin-3-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=C(C=CC=3)C=3C=NC=CC=3)N=CC=2)=CC=C1OC1CCOCC1 CZFNMENEUSTMAC-UHFFFAOYSA-N 0.000 claims description 2
BIYVUNBONXFTNM-UHFFFAOYSA-N 2-(oxan-4-yloxy)-5-[2-(3-pyridin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=C(C=CC=3)C=3C=CN=CC=3)N=CC=2)=CC=C1OC1CCOCC1 BIYVUNBONXFTNM-UHFFFAOYSA-N 0.000 claims description 2
LDHQCAZVNWUNTQ-UHFFFAOYSA-N 2-(oxan-4-yloxy)-5-[2-(4-pyridin-3-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=CC(=CC=3)C=3C=NC=CC=3)N=CC=2)=CC=C1OC1CCOCC1 LDHQCAZVNWUNTQ-UHFFFAOYSA-N 0.000 claims description 2
HDWLTQJKIPJSKY-UHFFFAOYSA-N 2-(oxan-4-yloxy)-5-[2-(4-pyridin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=CC(=CC=3)C=3C=CN=CC=3)N=CC=2)=CC=C1OC1CCOCC1 HDWLTQJKIPJSKY-UHFFFAOYSA-N 0.000 claims description 2
DOUZRYMTZGSGSY-UHFFFAOYSA-N 2-(oxan-4-yloxy)-5-[2-[3-(1,2,4-triazol-4-ylmethyl)anilino]pyrimidin-4-yl]benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=C(CN4C=NN=C4)C=CC=3)N=CC=2)=CC=C1OC1CCOCC1 DOUZRYMTZGSGSY-UHFFFAOYSA-N 0.000 claims description 2
KDBUKDMDYCBEGU-UHFFFAOYSA-N 2-(oxan-4-yloxy)-5-[2-[3-(2h-tetrazol-5-yl)anilino]pyrimidin-4-yl]benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=C(C=CC=3)C=3NN=NN=3)N=CC=2)=CC=C1OC1CCOCC1 KDBUKDMDYCBEGU-UHFFFAOYSA-N 0.000 claims description 2
PUTZAGSITKVLEL-UHFFFAOYSA-N 2-(oxan-4-yloxy)-5-[2-[3-(pyrrolidin-1-ylmethyl)anilino]pyrimidin-4-yl]benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=C(CN4CCCC4)C=CC=3)N=CC=2)=CC=C1OC1CCOCC1 PUTZAGSITKVLEL-UHFFFAOYSA-N 0.000 claims description 2
QRCHVBRWAOVMCV-UHFFFAOYSA-N 2-(oxan-4-yloxy)-5-[2-[3-(triazol-1-ylmethyl)anilino]pyrimidin-4-yl]benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=C(CN4N=NC=C4)C=CC=3)N=CC=2)=CC=C1OC1CCOCC1 QRCHVBRWAOVMCV-UHFFFAOYSA-N 0.000 claims description 2
PQPGOSUKJXTPRE-UHFFFAOYSA-N 2-(oxan-4-yloxy)-5-[2-[4-(1,2,4-triazol-1-yl)anilino]pyrimidin-4-yl]benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=CC(=CC=3)N3N=CN=C3)N=CC=2)=CC=C1OC1CCOCC1 PQPGOSUKJXTPRE-UHFFFAOYSA-N 0.000 claims description 2
AHGSZZFJHZMMDF-UHFFFAOYSA-N 2-(oxan-4-yloxy)-5-[2-[4-(1,2,4-triazol-1-ylmethyl)anilino]pyrimidin-4-yl]benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=CC(CN4N=CN=C4)=CC=3)N=CC=2)=CC=C1OC1CCOCC1 AHGSZZFJHZMMDF-UHFFFAOYSA-N 0.000 claims description 2
GSFZTTFAOPQXMF-UHFFFAOYSA-N 2-(oxan-4-yloxy)-5-[2-[4-(1,2,4-triazol-4-yl)anilino]pyrimidin-4-yl]benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=CC(=CC=3)N3C=NN=C3)N=CC=2)=CC=C1OC1CCOCC1 GSFZTTFAOPQXMF-UHFFFAOYSA-N 0.000 claims description 2
WYZMAMRJYCVYCZ-UHFFFAOYSA-N 2-(oxan-4-yloxy)-5-[2-[4-(1h-pyrazol-4-yl)anilino]pyrimidin-4-yl]benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=CC(=CC=3)C3=CNN=C3)N=CC=2)=CC=C1OC1CCOCC1 WYZMAMRJYCVYCZ-UHFFFAOYSA-N 0.000 claims description 2
MEEBLLZYWOZTIO-UHFFFAOYSA-N 2-(oxan-4-yloxy)-5-[2-[4-(pyrrolidin-1-ylsulfonylmethyl)anilino]pyrimidin-4-yl]benzonitrile Chemical compound C1CCCN1S(=O)(=O)CC(C=C1)=CC=C1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 MEEBLLZYWOZTIO-UHFFFAOYSA-N 0.000 claims description 2
AEALUIAAMIDZOG-UHFFFAOYSA-N 2-(oxan-4-yloxy)-5-[2-[4-(tetrazol-1-ylmethyl)anilino]pyrimidin-4-yl]benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=CC(CN4N=NN=C4)=CC=3)N=CC=2)=CC=C1OC1CCOCC1 AEALUIAAMIDZOG-UHFFFAOYSA-N 0.000 claims description 2
QCBRWIOWUOVNFQ-UHFFFAOYSA-N 2-[(1-methylsulfonylpiperidin-4-yl)methoxy]-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C1CN(S(=O)(=O)C)CCC1COC1=CC=C(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)C=C1C#N QCBRWIOWUOVNFQ-UHFFFAOYSA-N 0.000 claims description 2
OMTUTQGIIHZXJA-UHFFFAOYSA-N 2-[(2-methylpropan-2-yl)oxy]-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C1=C(C#N)C(OC(C)(C)C)=CC=C1C1=CC=NC(NC=2C=CC(=CC=2)N2CCOCC2)=N1 OMTUTQGIIHZXJA-UHFFFAOYSA-N 0.000 claims description 2
NNJQSWSIJXLCOO-UHFFFAOYSA-N 2-[(3-methyloxetan-3-yl)methoxy]-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C=1C=C(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)C=C(C#N)C=1OCC1(C)COC1 NNJQSWSIJXLCOO-UHFFFAOYSA-N 0.000 claims description 2
PMOSTPAIYDGYRX-JOCHJYFZSA-N 2-[(3r)-1-(2-hydroxyacetyl)pyrrolidin-3-yl]oxy-5-[2-(3-methoxy-4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C=1C=C(N2CCOCC2)C(OC)=CC=1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1O[C@@H]1CCN(C(=O)CO)C1 PMOSTPAIYDGYRX-JOCHJYFZSA-N 0.000 claims description 2
FRCJFVBWVUROIA-HSZRJFAPSA-N 2-[(3r)-1-(2-hydroxyacetyl)pyrrolidin-3-yl]oxy-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C1N(C(=O)CO)CC[C@H]1OC1=CC=C(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)C=C1C#N FRCJFVBWVUROIA-HSZRJFAPSA-N 0.000 claims description 2
ZCXHBLBRQKIWGR-JOCHJYFZSA-N 2-[(3r)-1-(2-hydroxyacetyl)pyrrolidin-3-yl]oxy-5-[2-[3-(3-methoxyazetidin-1-yl)anilino]pyrimidin-4-yl]benzonitrile Chemical compound C1C(OC)CN1C1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(O[C@H]3CN(CC3)C(=O)CO)=CC=2)C#N)=C1 ZCXHBLBRQKIWGR-JOCHJYFZSA-N 0.000 claims description 2
ROTQFTDVFLFWCI-XMMISQBUSA-N 2-[(3r)-1-(2-hydroxyacetyl)pyrrolidin-3-yl]oxy-5-[2-[3-(3-methoxypyrrolidin-1-yl)anilino]pyrimidin-4-yl]benzonitrile Chemical compound C1C(OC)CCN1C1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(O[C@H]3CN(CC3)C(=O)CO)=CC=2)C#N)=C1 ROTQFTDVFLFWCI-XMMISQBUSA-N 0.000 claims description 2
IQNARNCLXVGGTQ-BJKOFHAPSA-N 2-[(3r)-1-(2-hydroxyacetyl)pyrrolidin-3-yl]oxy-5-[2-[3-[(2s)-2-(hydroxymethyl)pyrrolidin-1-yl]anilino]pyrimidin-4-yl]benzonitrile Chemical compound OC[C@@H]1CCCN1C1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(O[C@H]3CN(CC3)C(=O)CO)=CC=2)C#N)=C1 IQNARNCLXVGGTQ-BJKOFHAPSA-N 0.000 claims description 2
IIUSJWDAUBYDDX-XMMPIXPASA-N 2-[(3r)-1-(2-hydroxyacetyl)pyrrolidin-3-yl]oxy-5-[2-[3-[(4-methylimidazol-1-yl)methyl]anilino]pyrimidin-4-yl]benzonitrile Chemical compound C1=NC(C)=CN1CC1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(O[C@H]3CN(CC3)C(=O)CO)=CC=2)C#N)=C1 IIUSJWDAUBYDDX-XMMPIXPASA-N 0.000 claims description 2
LGRZVMIEJJKDOX-RUZDIDTESA-N 2-[(3r)-1-(2-hydroxyacetyl)pyrrolidin-3-yl]oxy-5-[2-[3-[4-(2-hydroxyethyl)piperazin-1-yl]anilino]pyrimidin-4-yl]benzonitrile Chemical compound C1CN(CCO)CCN1C1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(O[C@H]3CN(CC3)C(=O)CO)=CC=2)C#N)=C1 LGRZVMIEJJKDOX-RUZDIDTESA-N 0.000 claims description 2
AXJXKOFVMXPBRU-HSZRJFAPSA-N 2-[(3r)-1-(2-hydroxyacetyl)pyrrolidin-3-yl]oxy-5-[2-[4-[(3-hydroxyazetidin-1-yl)methyl]anilino]pyrimidin-4-yl]benzonitrile Chemical compound C1N(C(=O)CO)CC[C@H]1OC1=CC=C(C=2N=C(NC=3C=CC(CN4CC(O)C4)=CC=3)N=CC=2)C=C1C#N AXJXKOFVMXPBRU-HSZRJFAPSA-N 0.000 claims description 2
CDQMMZLXCHBDIJ-HSZRJFAPSA-N 2-[(3r)-1-(2-hydroxyacetyl)pyrrolidin-3-yl]oxy-5-[2-[4-[(3-methoxyazetidin-1-yl)methyl]anilino]pyrimidin-4-yl]benzonitrile Chemical compound C1C(OC)CN1CC(C=C1)=CC=C1NC1=NC=CC(C=2C=C(C(O[C@H]3CN(CC3)C(=O)CO)=CC=2)C#N)=N1 CDQMMZLXCHBDIJ-HSZRJFAPSA-N 0.000 claims description 2
CXWSPQUXVADFCT-AREMUKBSSA-N 2-[(3r)-1-(2-hydroxyacetyl)pyrrolidin-3-yl]oxy-5-[2-[4-[[4-(2-hydroxyethyl)piperazin-1-yl]methyl]anilino]pyrimidin-4-yl]benzonitrile Chemical compound C1CN(CCO)CCN1CC(C=C1)=CC=C1NC1=NC=CC(C=2C=C(C(O[C@H]3CN(CC3)C(=O)CO)=CC=2)C#N)=N1 CXWSPQUXVADFCT-AREMUKBSSA-N 0.000 claims description 2
VRFUZCFXDSDOFU-UHFFFAOYSA-N 2-[1-(2-hydroxyacetyl)piperidin-4-yl]oxy-5-[2-(3-methoxy-4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C=1C=C(N2CCOCC2)C(OC)=CC=1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCN(C(=O)CO)CC1 VRFUZCFXDSDOFU-UHFFFAOYSA-N 0.000 claims description 2
YQWHXONABXSNOR-UHFFFAOYSA-N 2-[1-(2-hydroxyacetyl)piperidin-4-yl]oxy-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C1CN(C(=O)CO)CCC1OC1=CC=C(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)C=C1C#N YQWHXONABXSNOR-UHFFFAOYSA-N 0.000 claims description 2
PMOSTPAIYDGYRX-UHFFFAOYSA-N 2-[1-(2-hydroxyacetyl)pyrrolidin-3-yl]oxy-5-[2-(3-methoxy-4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C=1C=C(N2CCOCC2)C(OC)=CC=1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCN(C(=O)CO)C1 PMOSTPAIYDGYRX-UHFFFAOYSA-N 0.000 claims description 2
FRCJFVBWVUROIA-UHFFFAOYSA-N 2-[1-(2-hydroxyacetyl)pyrrolidin-3-yl]oxy-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C1N(C(=O)CO)CCC1OC1=CC=C(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)C=C1C#N FRCJFVBWVUROIA-UHFFFAOYSA-N 0.000 claims description 2
IOYKFHXNSDBYNP-HXUWFJFHSA-N 2-[1-[(2r)-2-hydroxypropanoyl]piperidin-4-yl]oxy-3-methoxy-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound COC1=CC(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)=CC(C#N)=C1OC1CCN(C(=O)[C@@H](C)O)CC1 IOYKFHXNSDBYNP-HXUWFJFHSA-N 0.000 claims description 2
UXSYWUXYXZGIOA-FQEVSTJZSA-N 2-[1-[(2s)-2-hydroxypropanoyl]piperidin-4-yl]oxy-5-[2-(3-methoxy-4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C=1C=C(N2CCOCC2)C(OC)=CC=1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCN(C(=O)[C@H](C)O)CC1 UXSYWUXYXZGIOA-FQEVSTJZSA-N 0.000 claims description 2
PVSLRTZLYXETDI-FQEVSTJZSA-N 2-[1-[(2s)-2-hydroxypropanoyl]piperidin-4-yl]oxy-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C1CN(C(=O)[C@@H](O)C)CCC1OC1=CC=C(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)C=C1C#N PVSLRTZLYXETDI-FQEVSTJZSA-N 0.000 claims description 2
MPDGWMAPGNMUCM-NRFANRHFSA-N 2-[1-[(2s)-2-hydroxypropanoyl]piperidin-4-yl]oxy-5-[2-[4-(4-methylpiperazine-1-carbonyl)anilino]pyrimidin-4-yl]benzonitrile Chemical compound C1CN(C(=O)[C@@H](O)C)CCC1OC1=CC=C(C=2N=C(NC=3C=CC(=CC=3)C(=O)N3CCN(C)CC3)N=CC=2)C=C1C#N MPDGWMAPGNMUCM-NRFANRHFSA-N 0.000 claims description 2
HGBDDSDGTZOSOH-UHFFFAOYSA-N 2-amino-n-[[4-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]phenyl]methyl]-1,3-thiazole-5-carboxamide Chemical compound S1C(N)=NC=C1C(=O)NCC(C=C1)=CC=C1NC1=NC=CC(C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=N1 HGBDDSDGTZOSOH-UHFFFAOYSA-N 0.000 claims description 2
HGFCAPIIYDPYNY-UHFFFAOYSA-N 2-cyclohexyloxy-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)=CC=C1OC1CCCCC1 HGFCAPIIYDPYNY-UHFFFAOYSA-N 0.000 claims description 2
QRFZFUUDEVRFEX-UHFFFAOYSA-N 2-fluoro-5-[2-(3,4,5-trimethoxyanilino)pyrimidin-4-yl]benzonitrile Chemical compound COC1=C(OC)C(OC)=CC(NC=2N=C(C=CN=2)C=2C=C(C(F)=CC=2)C#N)=C1 QRFZFUUDEVRFEX-UHFFFAOYSA-N 0.000 claims description 2
BZPQYMXLMNMXQR-UHFFFAOYSA-N 2-fluoro-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C1=C(C#N)C(F)=CC=C1C1=CC=NC(NC=2C=CC(=CC=2)N2CCOCC2)=N1 BZPQYMXLMNMXQR-UHFFFAOYSA-N 0.000 claims description 2
RCPJIKVMUZQEEV-UHFFFAOYSA-N 2-hydroxy-5-[2-[3-methoxy-4-(3-oxopiperazin-1-yl)anilino]pyrimidin-4-yl]benzonitrile Chemical compound C=1C=C(N2CC(=O)NCC2)C(OC)=CC=1NC(N=1)=NC=CC=1C1=CC=C(O)C(C#N)=C1 RCPJIKVMUZQEEV-UHFFFAOYSA-N 0.000 claims description 2
KLKLUAZFPXTQME-UHFFFAOYSA-N 2-methoxy-5-[2-(3,4,5-trimethoxyanilino)pyrimidin-4-yl]benzonitrile Chemical compound C1=C(C#N)C(OC)=CC=C1C1=CC=NC(NC=2C=C(OC)C(OC)=C(OC)C=2)=N1 KLKLUAZFPXTQME-UHFFFAOYSA-N 0.000 claims description 2
JEQROUYMKZOFMX-UHFFFAOYSA-N 2-methoxy-5-[2-(3-methoxy-4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound C1=C(C#N)C(OC)=CC=C1C1=CC=NC(NC=2C=C(OC)C(N3CCOCC3)=CC=2)=N1 JEQROUYMKZOFMX-UHFFFAOYSA-N 0.000 claims description 2
PMIGJMOYXZFHHQ-UHFFFAOYSA-N 2-methoxy-5-[2-[3-methoxy-4-(3-oxo-1,4-diazepan-1-yl)anilino]pyrimidin-4-yl]benzonitrile Chemical compound C1=C(C#N)C(OC)=CC=C1C1=CC=NC(NC=2C=C(OC)C(N3CC(=O)NCCC3)=CC=2)=N1 PMIGJMOYXZFHHQ-UHFFFAOYSA-N 0.000 claims description 2
YIGRGIPDUDYYJV-UHFFFAOYSA-N 2-methoxy-5-[2-[3-methoxy-4-(3-oxopiperazin-1-yl)anilino]pyrimidin-4-yl]benzonitrile Chemical compound C1=C(C#N)C(OC)=CC=C1C1=CC=NC(NC=2C=C(OC)C(N3CC(=O)NCC3)=CC=2)=N1 YIGRGIPDUDYYJV-UHFFFAOYSA-N 0.000 claims description 2
JEFAXHNIHLZLJU-UHFFFAOYSA-N 2-methoxy-5-[2-[3-methoxy-4-(4-methyl-3-oxopiperazin-1-yl)anilino]pyrimidin-4-yl]benzonitrile Chemical compound C1=C(C#N)C(OC)=CC=C1C1=CC=NC(NC=2C=C(OC)C(N3CC(=O)N(C)CC3)=CC=2)=N1 JEFAXHNIHLZLJU-UHFFFAOYSA-N 0.000 claims description 2
QCPHSBMNUVOGLQ-UHFFFAOYSA-N 2-propan-2-yloxy-5-[2-(3,4,5-trimethoxyanilino)pyrimidin-4-yl]benzonitrile Chemical compound COC1=C(OC)C(OC)=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC(C)C)=CC=2)C#N)=C1 QCPHSBMNUVOGLQ-UHFFFAOYSA-N 0.000 claims description 2
DODYTIHAVQXAPH-UHFFFAOYSA-N 3-(2-anilinopyrimidin-4-yl)benzonitrile Chemical compound N#CC1=CC=CC(C=2N=C(NC=3C=CC=CC=3)N=CC=2)=C1 DODYTIHAVQXAPH-UHFFFAOYSA-N 0.000 claims description 2
MFUSQZDCXOGCFT-UHFFFAOYSA-N 3-[2-(3-hydroxyanilino)pyrimidin-4-yl]benzonitrile Chemical compound OC1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C=CC=2)C#N)=C1 MFUSQZDCXOGCFT-UHFFFAOYSA-N 0.000 claims description 2
YICUDEIQZCMRSY-UHFFFAOYSA-N 3-[2-(4-hydroxyanilino)pyrimidin-4-yl]benzonitrile Chemical compound C1=CC(O)=CC=C1NC1=NC=CC(C=2C=C(C=CC=2)C#N)=N1 YICUDEIQZCMRSY-UHFFFAOYSA-N 0.000 claims description 2
NRSBYIGUZHAVJL-UHFFFAOYSA-N 3-[2-(4-methoxyanilino)pyrimidin-4-yl]benzonitrile Chemical compound C1=CC(OC)=CC=C1NC1=NC=CC(C=2C=C(C=CC=2)C#N)=N1 NRSBYIGUZHAVJL-UHFFFAOYSA-N 0.000 claims description 2
CTJGWNLQGNXOAY-UHFFFAOYSA-N 3-[2-(4-morpholin-4-ylanilino)-7h-purin-6-yl]benzonitrile Chemical compound N#CC1=CC=CC(C=2C=3N=CNC=3N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=2)=C1 CTJGWNLQGNXOAY-UHFFFAOYSA-N 0.000 claims description 2
YPERCQQYRIOTEN-UHFFFAOYSA-N 3-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]benzonitrile Chemical compound N#CC1=CC=CC(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)=C1 YPERCQQYRIOTEN-UHFFFAOYSA-N 0.000 claims description 2
MTSCJGZEYTXGQY-UHFFFAOYSA-N 3-[2-[3-(hydroxymethyl)-4-morpholin-4-ylanilino]pyrimidin-4-yl]benzonitrile Chemical compound C=1C=C(N2CCOCC2)C(CO)=CC=1NC(N=1)=NC=CC=1C1=CC=CC(C#N)=C1 MTSCJGZEYTXGQY-UHFFFAOYSA-N 0.000 claims description 2
NQHAFNZXEMXRFF-UHFFFAOYSA-N 3-[3-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]phenyl]-1,1-dimethylurea Chemical compound CN(C)C(=O)NC1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 NQHAFNZXEMXRFF-UHFFFAOYSA-N 0.000 claims description 2
KCKRLJIZCNVKRE-UHFFFAOYSA-N 3-[[4-(3-cyanophenyl)pyrimidin-2-yl]amino]benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C=CC=2)C#N)=C1 KCKRLJIZCNVKRE-UHFFFAOYSA-N 0.000 claims description 2
QBQYNPOIGDXOBA-UHFFFAOYSA-N 3-methoxy-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound COC1=CC(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)=CC(C#N)=C1OC1CCOCC1 QBQYNPOIGDXOBA-UHFFFAOYSA-N 0.000 claims description 2
QOWJJIRIEHZZFU-UHFFFAOYSA-N 3-methoxy-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]-2-piperidin-4-yloxybenzonitrile Chemical compound COC1=CC(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)=CC(C#N)=C1OC1CCNCC1 QOWJJIRIEHZZFU-UHFFFAOYSA-N 0.000 claims description 2
KRXFDFCEYKPHHZ-UHFFFAOYSA-N 4-[3-cyano-4-(oxan-4-yloxy)phenyl]-2-[4-[2-[2-(dimethylsulfamoylamino)ethoxy]ethoxy]-3-methoxyanilino]pyrimidine Chemical compound C1=C(OCCOCCNS(=O)(=O)N(C)C)C(OC)=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 KRXFDFCEYKPHHZ-UHFFFAOYSA-N 0.000 claims description 2
XDNNKRLPFHWQTF-UHFFFAOYSA-N 4-[[4-[3-cyano-4-(2-methylpropoxy)phenyl]pyrimidin-2-yl]amino]-n-(2-methoxyethyl)benzamide Chemical compound C1=CC(C(=O)NCCOC)=CC=C1NC1=NC=CC(C=2C=C(C(OCC(C)C)=CC=2)C#N)=N1 XDNNKRLPFHWQTF-UHFFFAOYSA-N 0.000 claims description 2
NNCIZMHIOXVKJI-UHFFFAOYSA-N 4-[[4-[3-cyano-4-(cyclopropylmethoxy)phenyl]pyrimidin-2-yl]amino]-n-(2-methoxyethyl)benzamide Chemical compound C1=CC(C(=O)NCCOC)=CC=C1NC1=NC=CC(C=2C=C(C(OCC3CC3)=CC=2)C#N)=N1 NNCIZMHIOXVKJI-UHFFFAOYSA-N 0.000 claims description 2
DUWNBOQVZCECEU-UHFFFAOYSA-N 4-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]-2-methoxybenzamide Chemical compound C1=C(C(N)=O)C(OC)=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 DUWNBOQVZCECEU-UHFFFAOYSA-N 0.000 claims description 2
IMJBWIHTJIPGIQ-UHFFFAOYSA-N 4-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]-n-(3-hydroxypropyl)-2-methoxybenzenesulfonamide Chemical compound C1=C(S(=O)(=O)NCCCO)C(OC)=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 IMJBWIHTJIPGIQ-UHFFFAOYSA-N 0.000 claims description 2
ZTKDCFULADXLJW-UHFFFAOYSA-N 4-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]-n-(3-imidazol-1-ylpropyl)-2-methoxybenzenesulfonamide Chemical compound C=1C=C(S(=O)(=O)NCCCN2C=NC=C2)C(OC)=CC=1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 ZTKDCFULADXLJW-UHFFFAOYSA-N 0.000 claims description 2
SJIKUTKXMKYTTP-UHFFFAOYSA-N 4-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]-n-[2-(diethylamino)ethyl]-2-methoxybenzamide Chemical compound C1=C(OC)C(C(=O)NCCN(CC)CC)=CC=C1NC1=NC=CC(C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=N1 SJIKUTKXMKYTTP-UHFFFAOYSA-N 0.000 claims description 2
XAXIBPFXBWPLTP-UHFFFAOYSA-N 4-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]-n-[2-(dimethylamino)ethyl]-2-methoxy-n-methylbenzamide Chemical compound C1=C(C(=O)N(C)CCN(C)C)C(OC)=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 XAXIBPFXBWPLTP-UHFFFAOYSA-N 0.000 claims description 2
DGGPUHDBBWHXOP-UHFFFAOYSA-N 4-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]-n-[2-(dimethylamino)ethyl]-2-methoxybenzamide Chemical compound C1=C(C(=O)NCCN(C)C)C(OC)=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 DGGPUHDBBWHXOP-UHFFFAOYSA-N 0.000 claims description 2
WHTPRKDFROYAPF-UHFFFAOYSA-N 4-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]-n-[3-(dimethylamino)propyl]-2-methoxy-n-methylbenzenesulfonamide Chemical compound C1=C(S(=O)(=O)N(C)CCCN(C)C)C(OC)=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 WHTPRKDFROYAPF-UHFFFAOYSA-N 0.000 claims description 2
FNBZHORXCRXBSR-NRFANRHFSA-N 4-[[4-[3-cyano-4-[1-[(2s)-2-hydroxypropanoyl]piperidin-4-yl]oxyphenyl]pyrimidin-2-yl]amino]-n-[2-(dimethylamino)ethyl]-n-methylbenzamide Chemical compound C1CN(C(=O)[C@@H](O)C)CCC1OC1=CC=C(C=2N=C(NC=3C=CC(=CC=3)C(=O)N(C)CCN(C)C)N=CC=2)C=C1C#N FNBZHORXCRXBSR-NRFANRHFSA-N 0.000 claims description 2
DAEKNLNITYDYHH-NRFANRHFSA-N 4-[[4-[3-cyano-4-[1-[(2s)-2-hydroxypropanoyl]piperidin-4-yl]oxyphenyl]pyrimidin-2-yl]amino]-n-[3-(dimethylamino)propyl]-2-methoxybenzamide Chemical compound C1=C(C(=O)NCCCN(C)C)C(OC)=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCN(CC3)C(=O)[C@H](C)O)=CC=2)C#N)=C1 DAEKNLNITYDYHH-NRFANRHFSA-N 0.000 claims description 2
JXOIIZFZSFVRKX-UHFFFAOYSA-N 5-[2-(1,3-benzothiazol-5-ylamino)pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=C4N=CSC4=CC=3)N=CC=2)=CC=C1OC1CCOCC1 JXOIIZFZSFVRKX-UHFFFAOYSA-N 0.000 claims description 2
UGSIZGNZHGGZCQ-UHFFFAOYSA-N 5-[2-(1,3-benzothiazol-6-ylamino)pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=C4SC=NC4=CC=3)N=CC=2)=CC=C1OC1CCOCC1 UGSIZGNZHGGZCQ-UHFFFAOYSA-N 0.000 claims description 2
IIJDLQCTACFXSI-UHFFFAOYSA-N 5-[2-(3,4-dimethoxyanilino)pyrimidin-4-yl]-2-(dimethylamino)benzonitrile Chemical compound C1=C(OC)C(OC)=CC=C1NC1=NC=CC(C=2C=C(C(N(C)C)=CC=2)C#N)=N1 IIJDLQCTACFXSI-UHFFFAOYSA-N 0.000 claims description 2
NWXWWPDHPXAROR-UHFFFAOYSA-N 5-[2-(3,4-dimethoxyanilino)pyrimidin-4-yl]-2-(methylamino)benzonitrile Chemical compound C1=C(C#N)C(NC)=CC=C1C1=CC=NC(NC=2C=C(OC)C(OC)=CC=2)=N1 NWXWWPDHPXAROR-UHFFFAOYSA-N 0.000 claims description 2
HDMHIHMCJJCAAI-UHFFFAOYSA-N 5-[2-(3,4-dimethoxyanilino)pyrimidin-4-yl]-2-hydroxybenzonitrile Chemical compound C1=C(OC)C(OC)=CC=C1NC1=NC=CC(C=2C=C(C(O)=CC=2)C#N)=N1 HDMHIHMCJJCAAI-UHFFFAOYSA-N 0.000 claims description 2
OJGPEADLSPBSQH-UHFFFAOYSA-N 5-[2-(3,4-dimethoxyanilino)pyrimidin-4-yl]-2-propan-2-yloxybenzonitrile Chemical compound C1=C(OC)C(OC)=CC=C1NC1=NC=CC(C=2C=C(C(OC(C)C)=CC=2)C#N)=N1 OJGPEADLSPBSQH-UHFFFAOYSA-N 0.000 claims description 2
YYEDCODVAQLBDK-OAQYLSRUSA-N 5-[2-(3,4-dimethylanilino)pyrimidin-4-yl]-2-[(3r)-1-(2-hydroxyacetyl)pyrrolidin-3-yl]oxybenzonitrile Chemical compound C1=C(C)C(C)=CC=C1NC1=NC=CC(C=2C=C(C(O[C@H]3CN(CC3)C(=O)CO)=CC=2)C#N)=N1 YYEDCODVAQLBDK-OAQYLSRUSA-N 0.000 claims description 2
CZVCMZDZAWJEPZ-UHFFFAOYSA-N 5-[2-(3,5-dimethylanilino)pyrimidin-4-yl]-2-ethoxybenzonitrile Chemical compound C1=C(C#N)C(OCC)=CC=C1C1=CC=NC(NC=2C=C(C)C=C(C)C=2)=N1 CZVCMZDZAWJEPZ-UHFFFAOYSA-N 0.000 claims description 2
WVKLLJVWOPMMCZ-UHFFFAOYSA-N 5-[2-(3-aminoanilino)pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound NC1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 WVKLLJVWOPMMCZ-UHFFFAOYSA-N 0.000 claims description 2
UQNNKNKAKAUWBL-UHFFFAOYSA-N 5-[2-(3-chloro-4-morpholin-4-ylanilino)pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C=1C=C(N2CCOCC2)C(Cl)=CC=1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 UQNNKNKAKAUWBL-UHFFFAOYSA-N 0.000 claims description 2
VWUBQMKHFPPHOK-UHFFFAOYSA-N 5-[2-(3-chloro-4-morpholin-4-ylanilino)pyrimidin-4-yl]-2-methoxybenzonitrile Chemical compound C1=C(C#N)C(OC)=CC=C1C1=CC=NC(NC=2C=C(Cl)C(N3CCOCC3)=CC=2)=N1 VWUBQMKHFPPHOK-UHFFFAOYSA-N 0.000 claims description 2
APNWBGWCAOYDNF-UHFFFAOYSA-N 5-[2-(3-cyclopropyl-4-morpholin-4-ylanilino)pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=C(C(N4CCOCC4)=CC=3)C3CC3)N=CC=2)=CC=C1OC1CCOCC1 APNWBGWCAOYDNF-UHFFFAOYSA-N 0.000 claims description 2
IOHDCWLNHPHVTE-OAQYLSRUSA-N 5-[2-(3-ethylanilino)pyrimidin-4-yl]-2-[(3r)-1-(2-hydroxyacetyl)pyrrolidin-3-yl]oxybenzonitrile Chemical compound CCC1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(O[C@H]3CN(CC3)C(=O)CO)=CC=2)C#N)=C1 IOHDCWLNHPHVTE-OAQYLSRUSA-N 0.000 claims description 2
VQZKYGKNDYNMCT-UHFFFAOYSA-N 5-[2-(3-fluoro-4-morpholin-4-ylanilino)pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C=1C=C(N2CCOCC2)C(F)=CC=1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 VQZKYGKNDYNMCT-UHFFFAOYSA-N 0.000 claims description 2
IHZIZBJEHMBSJN-UHFFFAOYSA-N 5-[2-(3-imidazol-1-ylanilino)pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=C(C=CC=3)N3C=NC=C3)N=CC=2)=CC=C1OC1CCOCC1 IHZIZBJEHMBSJN-UHFFFAOYSA-N 0.000 claims description 2
HPXHSJQOUDUPNZ-UHFFFAOYSA-N 5-[2-(3-methoxy-4-morpholin-4-ylanilino)pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C=1C=C(N2CCOCC2)C(OC)=CC=1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 HPXHSJQOUDUPNZ-UHFFFAOYSA-N 0.000 claims description 2
LXJZDGHYPWGKLG-UHFFFAOYSA-N 5-[2-(3-methoxy-4-pyrrolidin-1-ylsulfonylanilino)pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C=1C=C(S(=O)(=O)N2CCCC2)C(OC)=CC=1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 LXJZDGHYPWGKLG-UHFFFAOYSA-N 0.000 claims description 2
BOWRCZCTNOCIQE-UHFFFAOYSA-N 5-[2-(3-methyl-4-morpholin-4-ylanilino)pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C=1C=C(N2CCOCC2)C(C)=CC=1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 BOWRCZCTNOCIQE-UHFFFAOYSA-N 0.000 claims description 2
DOJCXPOCXYIRSH-UHFFFAOYSA-N 5-[2-(3h-benzimidazol-5-ylamino)pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=C4N=CNC4=CC=3)N=CC=2)=CC=C1OC1CCOCC1 DOJCXPOCXYIRSH-UHFFFAOYSA-N 0.000 claims description 2
VJFNZKPXRNKPOE-UHFFFAOYSA-N 5-[2-(4-aminoanilino)pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1=CC(N)=CC=C1NC1=NC=CC(C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=N1 VJFNZKPXRNKPOE-UHFFFAOYSA-N 0.000 claims description 2
WEXPZTIXVPLLME-UHFFFAOYSA-N 5-[2-(4-fluoro-3-pyrrolidin-3-yloxyanilino)pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1=C(OC2CNCC2)C(F)=CC=C1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 WEXPZTIXVPLLME-UHFFFAOYSA-N 0.000 claims description 2
KTMCVERMQSGGFO-UHFFFAOYSA-N 5-[2-(4-hydroxy-3-methoxyanilino)pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1=C(O)C(OC)=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 KTMCVERMQSGGFO-UHFFFAOYSA-N 0.000 claims description 2
DZVGIGQBTJWCDQ-UHFFFAOYSA-N 5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]-2-(oxan-4-ylmethoxy)benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)=CC=C1OCC1CCOCC1 DZVGIGQBTJWCDQ-UHFFFAOYSA-N 0.000 claims description 2
BWABTWGSXHTHCG-UHFFFAOYSA-N 5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)=CC=C1OC1CCOCC1 BWABTWGSXHTHCG-UHFFFAOYSA-N 0.000 claims description 2
GFLAYCQBSVDICX-UHFFFAOYSA-N 5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]-2-(oxolan-3-yloxy)benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)=CC=C1OC1CCOC1 GFLAYCQBSVDICX-UHFFFAOYSA-N 0.000 claims description 2
MPTVJPRFJWNQTN-UHFFFAOYSA-N 5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]-2-(piperidin-4-ylmethoxy)benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)=CC=C1OCC1CCNCC1 MPTVJPRFJWNQTN-UHFFFAOYSA-N 0.000 claims description 2
XHBHLSFBDPIANS-UHFFFAOYSA-N 5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]-2-(propan-2-ylamino)benzonitrile Chemical compound C1=C(C#N)C(NC(C)C)=CC=C1C1=CC=NC(NC=2C=CC(=CC=2)N2CCOCC2)=N1 XHBHLSFBDPIANS-UHFFFAOYSA-N 0.000 claims description 2
PPCPJKIBDULVJI-UHFFFAOYSA-N 5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]-2-propan-2-yloxybenzonitrile Chemical compound C1=C(C#N)C(OC(C)C)=CC=C1C1=CC=NC(NC=2C=CC(=CC=2)N2CCOCC2)=N1 PPCPJKIBDULVJI-UHFFFAOYSA-N 0.000 claims description 2
PHLJUFARQMNCBI-UHFFFAOYSA-N 5-[2-[3-(2,3-dihydroxypropoxy)-4-fluoroanilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1=C(F)C(OCC(O)CO)=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 PHLJUFARQMNCBI-UHFFFAOYSA-N 0.000 claims description 2
RHELWWBGOLRMSR-UHFFFAOYSA-N 5-[2-[3-(2-aminoethoxy)-4-fluoroanilino]pyrimidin-4-yl]-2-(cyclopropylmethoxy)benzonitrile Chemical compound C1=C(F)C(OCCN)=CC(NC=2N=C(C=CN=2)C=2C=C(C(OCC3CC3)=CC=2)C#N)=C1 RHELWWBGOLRMSR-UHFFFAOYSA-N 0.000 claims description 2
JLUYKNWFIXUIOK-UHFFFAOYSA-N 5-[2-[3-(2-aminoethoxy)-4-fluoroanilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1=C(F)C(OCCN)=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 JLUYKNWFIXUIOK-UHFFFAOYSA-N 0.000 claims description 2
HFGNCLNJZNXATG-KRWDZBQOSA-N 5-[2-[3-(2-aminoethoxy)-4-fluoroanilino]pyrimidin-4-yl]-2-[1-[(2s)-2-hydroxypropanoyl]piperidin-4-yl]oxybenzonitrile Chemical compound C1CN(C(=O)[C@@H](O)C)CCC1OC1=CC=C(C=2N=C(NC=3C=C(OCCN)C(F)=CC=3)N=CC=2)C=C1C#N HFGNCLNJZNXATG-KRWDZBQOSA-N 0.000 claims description 2
QSASCSMXGGTPDY-UHFFFAOYSA-N 5-[2-[3-(2-aminoethoxy)-4-methylanilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1=C(OCCN)C(C)=CC=C1NC1=NC=CC(C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=N1 QSASCSMXGGTPDY-UHFFFAOYSA-N 0.000 claims description 2
VTGLAUWOMWNGQO-UHFFFAOYSA-N 5-[2-[3-(2-morpholin-4-ylethoxy)anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=C(OCCN4CCOCC4)C=CC=3)N=CC=2)=CC=C1OC1CCOCC1 VTGLAUWOMWNGQO-UHFFFAOYSA-N 0.000 claims description 2
OYYUJDWKIKRWBJ-UHFFFAOYSA-N 5-[2-[3-(2-morpholin-4-ylethylamino)anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=C(NCCN4CCOCC4)C=CC=3)N=CC=2)=CC=C1OC1CCOCC1 OYYUJDWKIKRWBJ-UHFFFAOYSA-N 0.000 claims description 2
GLYTVSZNFMDENG-UHFFFAOYSA-N 5-[2-[3-(3-methoxyazetidin-1-yl)-4-methylanilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1C(OC)CN1C1=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=CC=C1C GLYTVSZNFMDENG-UHFFFAOYSA-N 0.000 claims description 2
NGBSZIMQAXEKHO-UHFFFAOYSA-N 5-[2-[3-(dimethylamino)anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound CN(C)C1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 NGBSZIMQAXEKHO-UHFFFAOYSA-N 0.000 claims description 2
BXLPGIULXMQEQP-UHFFFAOYSA-N 5-[2-[3-(hydroxymethyl)-4,5-dimethoxyanilino]pyrimidin-4-yl]-2-methoxybenzonitrile Chemical compound C1=C(C#N)C(OC)=CC=C1C1=CC=NC(NC=2C=C(OC)C(OC)=C(CO)C=2)=N1 BXLPGIULXMQEQP-UHFFFAOYSA-N 0.000 claims description 2
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FSODMMPATRLNRO-UHFFFAOYSA-N 5-[2-[3-[(3-hydroxypyrrolidin-1-yl)methyl]anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1C(O)CCN1CC1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 FSODMMPATRLNRO-UHFFFAOYSA-N 0.000 claims description 2
SBHWJTGOVKWGSN-UHFFFAOYSA-N 5-[2-[3-[(dimethylamino)methyl]anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound CN(C)CC1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 SBHWJTGOVKWGSN-UHFFFAOYSA-N 0.000 claims description 2
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RQOWKRYIVDFDNU-UHFFFAOYSA-N 5-[2-[4-[(2-methoxyethylamino)methyl]anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1=CC(CNCCOC)=CC=C1NC1=NC=CC(C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=N1 RQOWKRYIVDFDNU-UHFFFAOYSA-N 0.000 claims description 2
ZVWFGFHHHCLEFK-UHFFFAOYSA-N 5-[2-[4-[(2-methylimidazol-1-yl)methyl]anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound CC1=NC=CN1CC(C=C1)=CC=C1NC1=NC=CC(C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=N1 ZVWFGFHHHCLEFK-UHFFFAOYSA-N 0.000 claims description 2
JEWYHCPXSQFKLH-UHFFFAOYSA-N 5-[2-[4-[(3-hydroxyazetidin-1-yl)methyl]anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1C(O)CN1CC(C=C1)=CC=C1NC1=NC=CC(C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=N1 JEWYHCPXSQFKLH-UHFFFAOYSA-N 0.000 claims description 2
IDCRDDAWTMSRAI-UHFFFAOYSA-N 5-[2-[4-[(3-methoxyazetidin-1-yl)methyl]anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1C(OC)CN1CC(C=C1)=CC=C1NC1=NC=CC(C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=N1 IDCRDDAWTMSRAI-UHFFFAOYSA-N 0.000 claims description 2
AZBIISDQFQRSTM-OWOJBTEDSA-N 5-[2-[4-[(e)-3-morpholin-4-ylprop-1-enyl]anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound N#CC1=CC(C=2N=C(NC=3C=CC(\C=C\CN4CCOCC4)=CC=3)N=CC=2)=CC=C1OC1CCOCC1 AZBIISDQFQRSTM-OWOJBTEDSA-N 0.000 claims description 2
JEAICYDMJHKLPS-UHFFFAOYSA-N 5-[2-[4-[1-(3-methoxyazetidin-1-yl)ethyl]anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1C(OC)CN1C(C)C(C=C1)=CC=C1NC1=NC=CC(C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=N1 JEAICYDMJHKLPS-UHFFFAOYSA-N 0.000 claims description 2
MEFZGBDNJAHDJN-UHFFFAOYSA-N 5-[2-[4-[2-(2-aminoethoxy)ethoxy]-3-methoxyanilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1=C(OCCOCCN)C(OC)=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 MEFZGBDNJAHDJN-UHFFFAOYSA-N 0.000 claims description 2
JAVVRJMEPJMVHH-UHFFFAOYSA-N 5-[2-[4-[2-(diethylamino)ethoxy]-3-methoxyanilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1=C(OC)C(OCCN(CC)CC)=CC=C1NC1=NC=CC(C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=N1 JAVVRJMEPJMVHH-UHFFFAOYSA-N 0.000 claims description 2
YPTJLLMDWKTGCC-UHFFFAOYSA-N 5-[2-[4-[3-(dimethylamino)azetidine-1-carbonyl]-3-methoxyanilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C=1C=C(C(=O)N2CC(C2)N(C)C)C(OC)=CC=1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 YPTJLLMDWKTGCC-UHFFFAOYSA-N 0.000 claims description 2
MDNCSQVIANBCOM-UHFFFAOYSA-N 5-[2-[4-[3-(dimethylamino)pyrrolidin-1-yl]sulfonyl-3-methoxyanilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C=1C=C(S(=O)(=O)N2CC(CC2)N(C)C)C(OC)=CC=1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 MDNCSQVIANBCOM-UHFFFAOYSA-N 0.000 claims description 2
NGYCGEUKCIDHSG-UHFFFAOYSA-N 5-[2-[4-[3-[(dimethylamino)methyl]azetidine-1-carbonyl]-3-methoxyanilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C=1C=C(C(=O)N2CC(CN(C)C)C2)C(OC)=CC=1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 NGYCGEUKCIDHSG-UHFFFAOYSA-N 0.000 claims description 2
AFWFSLVMXBTGRN-UHFFFAOYSA-N 5-[2-[4-[4-(2-hydroxyethyl)piperazin-1-yl]anilino]pyrimidin-4-yl]-2-(2-methylpropoxy)benzonitrile Chemical compound C1=C(C#N)C(OCC(C)C)=CC=C1C1=CC=NC(NC=2C=CC(=CC=2)N2CCN(CCO)CC2)=N1 AFWFSLVMXBTGRN-UHFFFAOYSA-N 0.000 claims description 2
XAWFXIHGRUCOOR-UHFFFAOYSA-N 5-[2-[4-[4-(2-hydroxyethyl)piperazin-1-yl]anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1CN(CCO)CCN1C(C=C1)=CC=C1NC1=NC=CC(C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=N1 XAWFXIHGRUCOOR-UHFFFAOYSA-N 0.000 claims description 2
YNVVVZBCORLISK-UHFFFAOYSA-N 5-[2-[4-[4-(2-hydroxyethyl)piperazin-1-yl]anilino]pyrimidin-4-yl]-2-[(3-methyloxetan-3-yl)methoxy]benzonitrile Chemical compound C=1C=C(C=2N=C(NC=3C=CC(=CC=3)N3CCN(CCO)CC3)N=CC=2)C=C(C#N)C=1OCC1(C)COC1 YNVVVZBCORLISK-UHFFFAOYSA-N 0.000 claims description 2
XDKGLOMIIQBBCB-UHFFFAOYSA-N 5-[2-[4-[4-(2-hydroxyethyl)piperazin-1-yl]anilino]pyrimidin-4-yl]-3-methoxy-2-(oxan-4-yloxy)benzonitrile Chemical compound COC1=CC(C=2N=C(NC=3C=CC(=CC=3)N3CCN(CCO)CC3)N=CC=2)=CC(C#N)=C1OC1CCOCC1 XDKGLOMIIQBBCB-UHFFFAOYSA-N 0.000 claims description 2
ZZMJIGOBEPEDFV-UHFFFAOYSA-N 5-[2-[4-[4-(2-hydroxyethyl)piperazine-1-carbonyl]-3-methoxyanilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C=1C=C(C(=O)N2CCN(CCO)CC2)C(OC)=CC=1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 ZZMJIGOBEPEDFV-UHFFFAOYSA-N 0.000 claims description 2
HVISCZVTQDXEPD-UHFFFAOYSA-N 5-[2-[4-[[4-(2-hydroxyethyl)piperazin-1-yl]methyl]-3-methoxyanilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C=1C=C(CN2CCN(CCO)CC2)C(OC)=CC=1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 HVISCZVTQDXEPD-UHFFFAOYSA-N 0.000 claims description 2
FBFRLOMDXVELRT-UHFFFAOYSA-N 5-[2-[4-fluoro-3-(2-piperazin-1-ylethoxy)anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1=C(OCCN2CCNCC2)C(F)=CC=C1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 FBFRLOMDXVELRT-UHFFFAOYSA-N 0.000 claims description 2
JWHUBYIVMTXMQB-UHFFFAOYSA-N 5-[2-[4-fluoro-3-(3-morpholin-4-ylpropoxy)anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1=C(OCCCN2CCOCC2)C(F)=CC=C1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 JWHUBYIVMTXMQB-UHFFFAOYSA-N 0.000 claims description 2
IFZQENAVDIXSSW-UHFFFAOYSA-N 5-[2-[4-fluoro-3-[2-(4-propan-2-ylpiperazin-1-yl)ethoxy]anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1CN(C(C)C)CCN1CCOC1=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=CC=C1F IFZQENAVDIXSSW-UHFFFAOYSA-N 0.000 claims description 2
BOGVKGJQQIWUNR-UHFFFAOYSA-N 5-[2-[4-methoxy-3-(3-morpholin-4-ylpropoxy)anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1=C(OCCCN2CCOCC2)C(OC)=CC=C1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 BOGVKGJQQIWUNR-UHFFFAOYSA-N 0.000 claims description 2
ILUZSBGQHXVWSJ-UHFFFAOYSA-N 5-[2-[4-methoxy-3-(3-piperazin-1-ylpropoxy)anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1=C(OCCCN2CCNCC2)C(OC)=CC=C1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 ILUZSBGQHXVWSJ-UHFFFAOYSA-N 0.000 claims description 2
XVPMVTKPWFMWHQ-UHFFFAOYSA-N 5-[2-[4-methoxy-3-(3-piperidin-4-ylpropoxy)anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1=C(OCCCC2CCNCC2)C(OC)=CC=C1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 XVPMVTKPWFMWHQ-UHFFFAOYSA-N 0.000 claims description 2
UMZKZMDPDIAXCY-UHFFFAOYSA-N 5-[2-[4-methoxy-3-[3-(4-propan-2-ylpiperazin-1-yl)propoxy]anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1=C(OCCCN2CCN(CC2)C(C)C)C(OC)=CC=C1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 UMZKZMDPDIAXCY-UHFFFAOYSA-N 0.000 claims description 2
PXNVILCNGSPEMM-UHFFFAOYSA-N 5-[2-[4-methoxy-3-[3-[4-(2-methylpropanoyl)piperazin-1-yl]propoxy]anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1=C(OCCCN2CCN(CC2)C(=O)C(C)C)C(OC)=CC=C1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 PXNVILCNGSPEMM-UHFFFAOYSA-N 0.000 claims description 2
FXXGLCKUZJOZRE-UHFFFAOYSA-N 5-[2-[4-methyl-3-(2-piperazin-1-ylethoxy)anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1=C(OCCN2CCNCC2)C(C)=CC=C1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 FXXGLCKUZJOZRE-UHFFFAOYSA-N 0.000 claims description 2
ORVZLPXLDOLHEU-UHFFFAOYSA-N 5-[2-[4-methyl-3-(3-morpholin-4-ylpropoxy)anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1=C(OCCCN2CCOCC2)C(C)=CC=C1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 ORVZLPXLDOLHEU-UHFFFAOYSA-N 0.000 claims description 2
JYQBBDVKLTZIQT-UHFFFAOYSA-N 5-[2-[4-methyl-3-[2-(4-propan-2-ylpiperazin-1-yl)ethoxy]anilino]pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound C1CN(C(C)C)CCN1CCOC1=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=CC=C1C JYQBBDVKLTZIQT-UHFFFAOYSA-N 0.000 claims description 2
AAUBMMZCSXNVNV-UHFFFAOYSA-N 5-[5-fluoro-2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]-2-(oxan-4-yloxy)benzonitrile Chemical compound N1=C(C=2C=C(C(OC3CCOCC3)=CC=2)C#N)C(F)=CN=C1NC(C=C1)=CC=C1N1CCOCC1 AAUBMMZCSXNVNV-UHFFFAOYSA-N 0.000 claims description 2
KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 claims description 2
IWEWWZFSRUUELO-UHFFFAOYSA-N N#CC(C=CC=C1)=C1C1=NC(NC(C=C2)=CC=C2S(N(CC2)CCC2(CN2CCCC2)O)(=O)=O)=NC=C1 Chemical compound N#CC(C=CC=C1)=C1C1=NC(NC(C=C2)=CC=C2S(N(CC2)CCC2(CN2CCCC2)O)(=O)=O)=NC=C1 IWEWWZFSRUUELO-UHFFFAOYSA-N 0.000 claims description 2
239000000654 additive Substances 0.000 claims description 2
230000000996 additive effect Effects 0.000 claims description 2
QNAYBMKLOCPYGJ-UHFFFAOYSA-M alaninate Chemical compound CC(N)C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-M 0.000 claims description 2
125000005081 alkoxyalkoxyalkyl group Chemical group 0.000 claims description 2
125000006350 alkyl thio alkyl group Chemical group 0.000 claims description 2
125000002431 aminoalkoxy group Chemical group 0.000 claims description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
125000004970 halomethyl group Chemical group 0.000 claims description 2
125000000592 heterocycloalkyl group Chemical group 0.000 claims description 2
210000005260 human cell Anatomy 0.000 claims description 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
WKIJSCYPPWGIDV-UHFFFAOYSA-N methyl 4-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]-2-methoxybenzoate Chemical compound C1=C(OC)C(C(=O)OC)=CC=C1NC1=NC=CC(C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=N1 WKIJSCYPPWGIDV-UHFFFAOYSA-N 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 2
ASFVKOYNTPOQKK-UHFFFAOYSA-N n-(1-methylpiperidin-4-yl)benzamide Chemical compound C1CN(C)CCC1NC(=O)C1=CC=CC=C1 ASFVKOYNTPOQKK-UHFFFAOYSA-N 0.000 claims description 2
PUDOBSLCLQHWOU-UHFFFAOYSA-N n-[2-[2-[4-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]-2-methoxyphenoxy]ethoxy]ethyl]-4-methylpiperazine-1-sulfonamide Chemical compound C=1C=C(OCCOCCNS(=O)(=O)N2CCN(C)CC2)C(OC)=CC=1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 PUDOBSLCLQHWOU-UHFFFAOYSA-N 0.000 claims description 2
OQALJZWMNMEYSW-UHFFFAOYSA-N n-[2-[2-[4-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]-2-methoxyphenoxy]ethoxy]ethyl]methanesulfonamide Chemical compound C1=C(OCCOCCNS(C)(=O)=O)C(OC)=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 OQALJZWMNMEYSW-UHFFFAOYSA-N 0.000 claims description 2
KCONINZVQOSEPF-UHFFFAOYSA-N n-[2-[2-[4-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]-2-methoxyphenoxy]ethoxy]ethyl]morpholine-4-sulfonamide Chemical compound C=1C=C(OCCOCCNS(=O)(=O)N2CCOCC2)C(OC)=CC=1NC(N=1)=NC=CC=1C(C=C1C#N)=CC=C1OC1CCOCC1 KCONINZVQOSEPF-UHFFFAOYSA-N 0.000 claims description 2
INBUNCTVJRKEOY-UHFFFAOYSA-N n-[2-cyano-4-[2-(3-methoxy-4-morpholin-4-ylanilino)pyrimidin-4-yl]phenyl]-2-methylpropanamide Chemical compound C=1C=C(N2CCOCC2)C(OC)=CC=1NC(N=1)=NC=CC=1C1=CC=C(NC(=O)C(C)C)C(C#N)=C1 INBUNCTVJRKEOY-UHFFFAOYSA-N 0.000 claims description 2
UWNJBUYXGUQPCS-UHFFFAOYSA-N n-[2-cyano-4-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]phenyl]-2-methylcyclopropane-1-carboxamide Chemical compound CC1CC1C(=O)NC1=CC=C(C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)C=C1C#N UWNJBUYXGUQPCS-UHFFFAOYSA-N 0.000 claims description 2
QQOUJCKXGZKYIS-UHFFFAOYSA-N n-[2-cyano-4-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]phenyl]-3,3,3-trifluoropropanamide Chemical compound C1=C(C#N)C(NC(=O)CC(F)(F)F)=CC=C1C1=CC=NC(NC=2C=CC(=CC=2)N2CCOCC2)=N1 QQOUJCKXGZKYIS-UHFFFAOYSA-N 0.000 claims description 2
ZXDCLOJVFHVDRH-UHFFFAOYSA-N n-[2-cyano-4-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]phenyl]-4-methylthiadiazole-5-carboxamide Chemical compound N1=NSC(C(=O)NC=2C(=CC(=CC=2)C=2N=C(NC=3C=CC(=CC=3)N3CCOCC3)N=CC=2)C#N)=C1C ZXDCLOJVFHVDRH-UHFFFAOYSA-N 0.000 claims description 2
OOFURRMHPBUVLN-UHFFFAOYSA-N n-[2-cyano-4-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]phenyl]cyclopropanecarboxamide Chemical compound C1CC1C(=O)NC(C(=C1)C#N)=CC=C1C(N=1)=CC=NC=1NC(C=C1)=CC=C1N1CCOCC1 OOFURRMHPBUVLN-UHFFFAOYSA-N 0.000 claims description 2
ACUBQQQOUVHULA-UHFFFAOYSA-N n-[2-cyano-4-[2-[3-(2-hydroxyethylsulfamoylmethyl)anilino]pyrimidin-4-yl]phenyl]cyclopropanecarboxamide Chemical compound OCCNS(=O)(=O)CC1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(NC(=O)C3CC3)=CC=2)C#N)=C1 ACUBQQQOUVHULA-UHFFFAOYSA-N 0.000 claims description 2
HUUQKZQWHXOJEH-UHFFFAOYSA-N n-[2-cyano-4-[2-[3-methoxy-4-(3-methoxyazetidine-1-carbonyl)anilino]pyrimidin-4-yl]phenyl]cyclopropanecarboxamide Chemical compound C1C(OC)CN1C(=O)C(C(=C1)OC)=CC=C1NC1=NC=CC(C=2C=C(C(NC(=O)C3CC3)=CC=2)C#N)=N1 HUUQKZQWHXOJEH-UHFFFAOYSA-N 0.000 claims description 2
DEZJLIJQKLGQLA-UHFFFAOYSA-N n-[2-cyano-4-[2-[3-methoxy-4-(3-oxopiperazin-1-yl)anilino]pyrimidin-4-yl]phenyl]-2-methylpropanamide Chemical compound C=1C=C(N2CC(=O)NCC2)C(OC)=CC=1NC(N=1)=NC=CC=1C1=CC=C(NC(=O)C(C)C)C(C#N)=C1 DEZJLIJQKLGQLA-UHFFFAOYSA-N 0.000 claims description 2
YESWBFHFESBTHX-UHFFFAOYSA-N n-[2-cyano-4-[2-[4-(2-hydroxyethylsulfamoylmethyl)anilino]pyrimidin-4-yl]phenyl]cyclopropanecarboxamide Chemical compound C1=CC(CS(=O)(=O)NCCO)=CC=C1NC1=NC=CC(C=2C=C(C(NC(=O)C3CC3)=CC=2)C#N)=N1 YESWBFHFESBTHX-UHFFFAOYSA-N 0.000 claims description 2
VZLIEWHUURUXKV-UHFFFAOYSA-N n-[2-cyano-4-[2-[4-(3-methoxyazetidine-1-carbonyl)anilino]pyrimidin-4-yl]phenyl]cyclopropanecarboxamide Chemical compound C1C(OC)CN1C(=O)C(C=C1)=CC=C1NC1=NC=CC(C=2C=C(C(NC(=O)C3CC3)=CC=2)C#N)=N1 VZLIEWHUURUXKV-UHFFFAOYSA-N 0.000 claims description 2
VYKJVVRURPBHRS-UHFFFAOYSA-N n-[3-[2-cyano-4-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]phenoxy]propyl]-2-hydroxyacetamide Chemical compound C1=C(C#N)C(OCCCNC(=O)CO)=CC=C1C1=CC=NC(NC=2C=CC(=CC=2)N2CCOCC2)=N1 VYKJVVRURPBHRS-UHFFFAOYSA-N 0.000 claims description 2
GEJCLXYBWJQEPB-UHFFFAOYSA-N n-[3-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]phenyl]-1-methylpyrazole-3-carboxamide Chemical compound CN1C=CC(C(=O)NC=2C=C(NC=3N=C(C=CN=3)C=3C=C(C(OC4CCOCC4)=CC=3)C#N)C=CC=2)=N1 GEJCLXYBWJQEPB-UHFFFAOYSA-N 0.000 claims description 2
MANDBVGBVPUUIH-UHFFFAOYSA-N n-[3-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]phenyl]-2-hydroxy-2-methylpropanamide Chemical compound CC(C)(O)C(=O)NC1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 MANDBVGBVPUUIH-UHFFFAOYSA-N 0.000 claims description 2
CYCVPYWCMNXRMA-UHFFFAOYSA-N n-[3-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]phenyl]-3-hydroxyazetidine-1-carboxamide Chemical compound C1C(O)CN1C(=O)NC1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 CYCVPYWCMNXRMA-UHFFFAOYSA-N 0.000 claims description 2
IMUQDWNDESEXRN-UHFFFAOYSA-N n-[3-[[4-[3-cyano-4-(oxan-4-yloxy)phenyl]pyrimidin-2-yl]amino]phenyl]-3-hydroxypyrrolidine-1-carboxamide Chemical compound C1C(O)CCN1C(=O)NC1=CC=CC(NC=2N=C(C=CN=2)C=2C=C(C(OC3CCOCC3)=CC=2)C#N)=C1 IMUQDWNDESEXRN-UHFFFAOYSA-N 0.000 claims description 2
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JP2012534299A 2009-10-12 2010-10-12 ＴＢＫ１および／またはＩＫＫεの阻害剤としてのアミノ−ピリミジン化合物 Pending JP2013507449A (ja)