JP2018516254A5 - - Google Patents
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- Publication number
- JP2018516254A5 JP2018516254A5 JP2017561653A JP2017561653A JP2018516254A5 JP 2018516254 A5 JP2018516254 A5 JP 2018516254A5 JP 2017561653 A JP2017561653 A JP 2017561653A JP 2017561653 A JP2017561653 A JP 2017561653A JP 2018516254 A5 JP2018516254 A5 JP 2018516254A5
- Authority
- JP
- Japan
- Prior art keywords
- pyrimidin
- amino
- methanone
- phenyl
- benzonitrile
- 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.)
- Pending
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- 150000003839 salts Chemical class 0.000 claims 10
- 150000001875 compounds Chemical class 0.000 claims 9
- 125000000623 heterocyclic group Chemical group 0.000 claims 9
- 125000005842 heteroatom Chemical group 0.000 claims 7
- -1 substituted Chemical class 0.000 claims 7
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 4
- 239000008194 pharmaceutical composition Substances 0.000 claims 3
- BZSFQWGXVZJHHW-UHFFFAOYSA-N (3-methylsulfonylphenyl)-[2-(pyrimidin-5-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound CS(=O)(=O)C=1C=C(C=CC=1)C(=O)C=1C=NC(=NC=1)NCC=1C=NC=NC=1 BZSFQWGXVZJHHW-UHFFFAOYSA-N 0.000 claims 2
- LOGKQBGLVHZLCP-UHFFFAOYSA-N (3-methylsulfonylphenyl)-[2-[(1-pyrimidin-5-ylcyclopropyl)amino]pyrimidin-5-yl]methanone Chemical compound CS(=O)(=O)C=1C=C(C=CC=1)C(=O)C=1C=NC(=NC=1)NC1(CC1)C=1C=NC=NC=1 LOGKQBGLVHZLCP-UHFFFAOYSA-N 0.000 claims 2
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 2
- PWNZBAASKKTHKD-UHFFFAOYSA-N 3-[2-(pyridin-3-ylmethylamino)pyrimidine-5-carbonyl]benzonitrile Chemical compound N1=CC(=CC=C1)CNC1=NC=C(C=N1)C(=O)C=1C=C(C#N)C=CC=1 PWNZBAASKKTHKD-UHFFFAOYSA-N 0.000 claims 2
- XFKDYJQBTISPOS-UHFFFAOYSA-N 3-[2-[(1-pyrazin-2-ylcyclopropyl)amino]pyrimidine-5-carbonyl]benzonitrile Chemical compound N1=C(C=NC=C1)C1(CC1)NC1=NC=C(C=N1)C(=O)C=1C=C(C#N)C=CC=1 XFKDYJQBTISPOS-UHFFFAOYSA-N 0.000 claims 2
- WLHYMEAMROQEIV-UHFFFAOYSA-N 3-[2-[(1-pyridin-3-ylcyclopropyl)amino]pyrimidine-5-carbonyl]benzonitrile Chemical compound N1=CC(=CC=C1)C1(CC1)NC1=NC=C(C=N1)C(=O)C=1C=C(C#N)C=CC=1 WLHYMEAMROQEIV-UHFFFAOYSA-N 0.000 claims 2
- OJUWWGHSEBTYGS-UHFFFAOYSA-N 3-[2-[(1-pyrimidin-5-ylcyclopropyl)amino]pyrimidine-5-carbonyl]benzonitrile Chemical compound N1=CN=CC(=C1)C1(CC1)NC1=NC=C(C=N1)C(=O)C=1C=C(C#N)C=CC=1 OJUWWGHSEBTYGS-UHFFFAOYSA-N 0.000 claims 2
- DRIOAXWEHSGQOM-UHFFFAOYSA-N 4-[[[5-[3-(trifluoromethyl)benzoyl]pyrimidin-2-yl]amino]methyl]benzamide Chemical compound FC(C=1C=C(C(=O)C=2C=NC(=NC=2)NCC2=CC=C(C(=O)N)C=C2)C=CC=1)(F)F DRIOAXWEHSGQOM-UHFFFAOYSA-N 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- VMVMHPUREDQQQA-UHFFFAOYSA-N [2-(pyrazin-2-ylmethylamino)pyrimidin-5-yl]-[3-(trifluoromethyl)phenyl]methanone Chemical compound N1=C(C=NC=C1)CNC1=NC=C(C=N1)C(=O)C1=CC(=CC=C1)C(F)(F)F VMVMHPUREDQQQA-UHFFFAOYSA-N 0.000 claims 2
- IKEXSEJPRXVFPJ-UHFFFAOYSA-N [2-(pyridin-3-ylmethylamino)pyrimidin-5-yl]-[3-(trifluoromethyl)phenyl]methanone Chemical compound N1=CC(=CC=C1)CNC1=NC=C(C=N1)C(=O)C1=CC(=CC=C1)C(F)(F)F IKEXSEJPRXVFPJ-UHFFFAOYSA-N 0.000 claims 2
- SNFIKXRRDPWTPT-UHFFFAOYSA-N [2-[(1-pyrimidin-5-ylcyclopropyl)amino]pyrimidin-5-yl]-[3-(trifluoromethyl)phenyl]methanone Chemical compound N1=CN=CC(=C1)C1(CC1)NC1=NC=C(C=N1)C(=O)C1=CC(=CC=C1)C(F)(F)F SNFIKXRRDPWTPT-UHFFFAOYSA-N 0.000 claims 2
- KBMLPTBEXTYAKP-UHFFFAOYSA-N [2-[(6-methylpyridin-3-yl)methylamino]pyrimidin-5-yl]-[3-(trifluoromethyl)phenyl]methanone Chemical compound CC1=CC=C(C=N1)CNC1=NC=C(C=N1)C(=O)C1=CC(=CC=C1)C(F)(F)F KBMLPTBEXTYAKP-UHFFFAOYSA-N 0.000 claims 2
- OIUSSRUDUJXLNH-UHFFFAOYSA-N [4-fluoro-3-(trifluoromethyl)phenyl]-[2-(pyridin-3-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound FC1=C(C=C(C=C1)C(=O)C=1C=NC(=NC=1)NCC=1C=NC=CC=1)C(F)(F)F OIUSSRUDUJXLNH-UHFFFAOYSA-N 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 201000010099 disease Diseases 0.000 claims 2
- 208000035475 disorder Diseases 0.000 claims 2
- 125000001475 halogen functional group Chemical group 0.000 claims 2
- 125000001072 heteroaryl group Chemical group 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 claims 2
- ZWFJYOCQOFGMLS-UHFFFAOYSA-N (1-methylindazol-5-yl)-[2-(pyrimidin-5-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound CN1N=CC2=CC(=CC=C12)C(=O)C=1C=NC(=NC=1)NCC=1C=NC=NC=1 ZWFJYOCQOFGMLS-UHFFFAOYSA-N 0.000 claims 1
- YHZVLKDGFBOZDR-UHFFFAOYSA-N (1-methylindazol-6-yl)-[2-(pyrimidin-5-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound CN1N=CC2=CC=C(C=C12)C(=O)C=1C=NC(=NC=1)NCC=1C=NC=NC=1 YHZVLKDGFBOZDR-UHFFFAOYSA-N 0.000 claims 1
- BAXFOZTZZUBQPS-UHFFFAOYSA-N (1-methylpyrazol-4-yl)-[2-(pyridin-3-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound CN1N=CC(=C1)C(=O)C=1C=NC(=NC=1)NCC=1C=NC=CC=1 BAXFOZTZZUBQPS-UHFFFAOYSA-N 0.000 claims 1
- QLEBCZCOYOABML-UHFFFAOYSA-N (2-chlorophenyl)-[2-(pyridin-3-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound ClC1=C(C=CC=C1)C(=O)C=1C=NC(=NC=1)NCC=1C=NC=CC=1 QLEBCZCOYOABML-UHFFFAOYSA-N 0.000 claims 1
- LHRALRNRTFSAFD-UHFFFAOYSA-N (2-fluorophenyl)-[2-(pyridin-3-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound FC1=C(C=CC=C1)C(=O)C=1C=NC(=NC=1)NCC=1C=NC=CC=1 LHRALRNRTFSAFD-UHFFFAOYSA-N 0.000 claims 1
- UDAOFNIBKHOPKM-UHFFFAOYSA-N (2-methylquinolin-6-yl)-[2-(pyridin-3-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound CC1=NC2=CC=C(C=C2C=C1)C(=O)C=1C=NC(=NC=1)NCC=1C=NC=CC=1 UDAOFNIBKHOPKM-UHFFFAOYSA-N 0.000 claims 1
- XVYVPEHJMUKZQA-UHFFFAOYSA-N (2-phenylmethoxypyrimidin-5-yl)-[3-(trifluoromethyl)phenyl]methanone Chemical compound C(C1=CC=CC=C1)OC1=NC=C(C=N1)C(=O)C1=CC(=CC=C1)C(F)(F)F XVYVPEHJMUKZQA-UHFFFAOYSA-N 0.000 claims 1
- YAAFHHBHGRNDAU-UHFFFAOYSA-N (3,4-difluorophenyl)-[2-(2-phenylpropan-2-ylamino)pyrimidin-5-yl]methanone Chemical compound FC=1C=C(C=CC=1F)C(=O)C=1C=NC(=NC=1)NC(C)(C)C1=CC=CC=C1 YAAFHHBHGRNDAU-UHFFFAOYSA-N 0.000 claims 1
- ORQAFBOXRPVLAZ-UHFFFAOYSA-N (3,4-difluorophenyl)-[2-(pyridin-3-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound FC=1C=C(C=CC=1F)C(=O)C=1C=NC(=NC=1)NCC=1C=NC=CC=1 ORQAFBOXRPVLAZ-UHFFFAOYSA-N 0.000 claims 1
- CBOTVXQGQFTLFC-UHFFFAOYSA-N (3,4-difluorophenyl)-[2-[(4-methoxyphenyl)methylamino]pyrimidin-5-yl]methanone Chemical compound FC=1C=C(C=CC=1F)C(=O)C=1C=NC(=NC=1)NCC1=CC=C(C=C1)OC CBOTVXQGQFTLFC-UHFFFAOYSA-N 0.000 claims 1
- CNHIYUMHLCGGJZ-UHFFFAOYSA-N (3-chlorophenyl)-[2-(2-phenylpropan-2-ylamino)pyrimidin-5-yl]methanone Chemical compound ClC=1C=C(C=CC=1)C(=O)C=1C=NC(=NC=1)NC(C)(C)C1=CC=CC=C1 CNHIYUMHLCGGJZ-UHFFFAOYSA-N 0.000 claims 1
- JYVRZPMQHRABJZ-UHFFFAOYSA-N (3-chlorophenyl)-[2-[(4-fluorophenyl)methylamino]pyrimidin-5-yl]methanone Chemical compound ClC=1C=C(C=CC=1)C(=O)C=1C=NC(=NC=1)NCC1=CC=C(C=C1)F JYVRZPMQHRABJZ-UHFFFAOYSA-N 0.000 claims 1
- HMEYDDDTXFFUAO-UHFFFAOYSA-N (3-methoxyphenyl)-[2-(1-pyrimidin-5-ylethylamino)pyrimidin-5-yl]methanone Chemical compound COC=1C=C(C=CC=1)C(=O)C=1C=NC(=NC=1)NC(C)C=1C=NC=NC=1 HMEYDDDTXFFUAO-UHFFFAOYSA-N 0.000 claims 1
- XSXULTISXSMVTK-UHFFFAOYSA-N (3-methoxyphenyl)-[2-(pyrimidin-5-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound COC=1C=C(C=CC=1)C(=O)C=1C=NC(=NC=1)NCC=1C=NC=NC=1 XSXULTISXSMVTK-UHFFFAOYSA-N 0.000 claims 1
- XISOVJXHGTWKNR-UHFFFAOYSA-N (3-methoxyphenyl)-[2-[(1-pyrimidin-5-ylcyclopropyl)amino]pyrimidin-5-yl]methanone Chemical compound COC=1C=C(C=CC=1)C(=O)C=1C=NC(=NC=1)NC1(CC1)C=1C=NC=NC=1 XISOVJXHGTWKNR-UHFFFAOYSA-N 0.000 claims 1
- PANWWXYCRZFFGW-UHFFFAOYSA-N (3-methylphenyl)-[2-(pyridin-2-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound CC=1C=C(C=CC=1)C(=O)C=1C=NC(=NC=1)NCC1=NC=CC=C1 PANWWXYCRZFFGW-UHFFFAOYSA-N 0.000 claims 1
- QUFWCLLJSUHQDF-UHFFFAOYSA-N (3-methylphenyl)-[2-(pyridin-3-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound CC=1C=C(C=CC=1)C(=O)C=1C=NC(=NC=1)NCC=1C=NC=CC=1 QUFWCLLJSUHQDF-UHFFFAOYSA-N 0.000 claims 1
- UIPITXGFIQSTPQ-UHFFFAOYSA-N (3-methylphenyl)-[2-(pyridin-4-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound CC=1C=C(C=CC=1)C(=O)C=1C=NC(=NC=1)NCC1=CC=NC=C1 UIPITXGFIQSTPQ-UHFFFAOYSA-N 0.000 claims 1
- FANUUQWWWRVXJE-UHFFFAOYSA-N (3-methylsulfonylphenyl)-[2-(pyridazin-3-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound CS(=O)(=O)C=1C=C(C=CC=1)C(=O)C=1C=NC(=NC=1)NCC=1N=NC=CC=1 FANUUQWWWRVXJE-UHFFFAOYSA-N 0.000 claims 1
- JWHGWYIWZYOKIO-UHFFFAOYSA-N (3-methylsulfonylphenyl)-[2-(pyridin-3-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound CS(=O)(=O)C=1C=C(C=CC=1)C(=O)C=1C=NC(=NC=1)NCC=1C=NC=CC=1 JWHGWYIWZYOKIO-UHFFFAOYSA-N 0.000 claims 1
- MSGNIYYOSFJXLG-UHFFFAOYSA-N (4-chlorophenyl)-[2-[(4-chlorophenyl)methylamino]pyrimidin-5-yl]methanone Chemical compound ClC1=CC=C(CNC2=NC=C(C=N2)C(=O)C2=CC=C(C=C2)Cl)C=C1 MSGNIYYOSFJXLG-UHFFFAOYSA-N 0.000 claims 1
- XOUQPSKQOSPKCW-UHFFFAOYSA-N (4-chlorophenyl)-[2-[(4-fluorophenyl)methylamino]pyrimidin-5-yl]methanone Chemical compound ClC1=CC=C(C=C1)C(=O)C=1C=NC(=NC=1)NCC1=CC=C(C=C1)F XOUQPSKQOSPKCW-UHFFFAOYSA-N 0.000 claims 1
- ZDZUFAZHYMTHTQ-UHFFFAOYSA-N (4-chlorophenyl)-[2-[(4-methoxyphenyl)methylamino]pyrimidin-5-yl]methanone Chemical compound ClC1=CC=C(C=C1)C(=O)C=1C=NC(=NC=1)NCC1=CC=C(C=C1)OC ZDZUFAZHYMTHTQ-UHFFFAOYSA-N 0.000 claims 1
- DLCJOHIRSZSWQF-UHFFFAOYSA-N (4-methoxyphenyl)-[2-(1-pyrimidin-5-ylethylamino)pyrimidin-5-yl]methanone Chemical compound COC1=CC=C(C=C1)C(=O)C=1C=NC(=NC=1)NC(C)C=1C=NC=NC=1 DLCJOHIRSZSWQF-UHFFFAOYSA-N 0.000 claims 1
- VCZLEUKDNDNGIU-UHFFFAOYSA-N (4-methoxyphenyl)-[2-(pyridin-2-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound COC1=CC=C(C=C1)C(=O)C=1C=NC(=NC=1)NCC1=NC=CC=C1 VCZLEUKDNDNGIU-UHFFFAOYSA-N 0.000 claims 1
- TYPBKMBMCQJTKB-UHFFFAOYSA-N (4-methoxyphenyl)-[2-[(4-methoxyphenyl)methylamino]pyrimidin-5-yl]methanone Chemical compound COC1=CC=C(CNC2=NC=C(C=N2)C(=O)C2=CC=C(C=C2)OC)C=C1 TYPBKMBMCQJTKB-UHFFFAOYSA-N 0.000 claims 1
- CCGPEEMOCCWEIQ-UHFFFAOYSA-N (4-methoxyphenyl)-[2-[[4-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]methanone Chemical compound COC1=CC=C(C=C1)C(=O)C=1C=NC(=NC=1)NCC1=CC=C(C=C1)OC(F)(F)F CCGPEEMOCCWEIQ-UHFFFAOYSA-N 0.000 claims 1
- BVAPXLVKROWRGH-UHFFFAOYSA-N 2,3-dihydro-1,4-benzodioxin-6-yl-[2-(2-phenylpropan-2-ylamino)pyrimidin-5-yl]methanone Chemical compound O1CCOC2=C1C=CC(=C2)C(=O)C=1C=NC(=NC=1)NC(C)(C)C1=CC=CC=C1 BVAPXLVKROWRGH-UHFFFAOYSA-N 0.000 claims 1
- KOOBRGTZZSEBQT-UHFFFAOYSA-N 2,3-dihydro-1,4-benzodioxin-6-yl-[2-(pyridin-3-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound O1CCOC2=C1C=CC(=C2)C(=O)C=1C=NC(=NC=1)NCC=1C=NC=CC=1 KOOBRGTZZSEBQT-UHFFFAOYSA-N 0.000 claims 1
- DLEUPGNCBIMSNI-UHFFFAOYSA-N 2-[3-[2-[(1-pyrimidin-5-ylcyclopropyl)amino]pyrimidine-5-carbonyl]phenyl]acetic acid Chemical compound N1=CN=CC(=C1)C1(CC1)NC1=NC=C(C=N1)C(=O)C=1C=C(C=CC=1)CC(=O)O DLEUPGNCBIMSNI-UHFFFAOYSA-N 0.000 claims 1
- MVXLTJGGEMJHMN-UHFFFAOYSA-N 2-chloro-5-[2-(pyrimidin-5-ylmethylamino)pyrimidine-5-carbonyl]benzonitrile Chemical compound ClC1=C(C#N)C=C(C=C1)C(=O)C=1C=NC(=NC=1)NCC=1C=NC=NC=1 MVXLTJGGEMJHMN-UHFFFAOYSA-N 0.000 claims 1
- UKDHZARBWOVIGP-UHFFFAOYSA-N 2-fluoro-5-[2-(pyrimidin-5-ylmethylamino)pyrimidine-5-carbonyl]benzonitrile Chemical compound FC1=C(C#N)C=C(C=C1)C(=O)C=1C=NC(=NC=1)NCC=1C=NC=NC=1 UKDHZARBWOVIGP-UHFFFAOYSA-N 0.000 claims 1
- HMMYJWHQXJQCAB-UHFFFAOYSA-N 2-methoxy-5-[2-[(1-pyrimidin-5-ylcyclopropyl)amino]pyrimidine-5-carbonyl]benzonitrile Chemical compound COC1=C(C#N)C=C(C=C1)C(=O)C=1C=NC(=NC=1)NC1(CC1)C=1C=NC=NC=1 HMMYJWHQXJQCAB-UHFFFAOYSA-N 0.000 claims 1
- KZQKRSJPAVTXSD-UHFFFAOYSA-N 2-methyl-5-[2-(pyrimidin-5-ylmethylamino)pyrimidine-5-carbonyl]benzonitrile Chemical compound CC1=C(C#N)C=C(C=C1)C(=O)C=1C=NC(=NC=1)NCC=1C=NC=NC=1 KZQKRSJPAVTXSD-UHFFFAOYSA-N 0.000 claims 1
- NMTUHPSKJJYGML-UHFFFAOYSA-N 3-(trifluoromethyl)benzaldehyde Chemical compound FC(F)(F)C1=CC=CC(C=O)=C1 NMTUHPSKJJYGML-UHFFFAOYSA-N 0.000 claims 1
- QALUXDRBPVQKBM-UHFFFAOYSA-N 3-[2-(1-pyridin-3-ylethylamino)pyrimidine-5-carbonyl]benzonitrile Chemical compound N1=CC(=CC=C1)C(C)NC1=NC=C(C=N1)C(=O)C=1C=C(C#N)C=CC=1 QALUXDRBPVQKBM-UHFFFAOYSA-N 0.000 claims 1
- VCAAYIIGVCSPBP-UHFFFAOYSA-N 3-[2-(2-phenylpropan-2-ylamino)pyrimidine-5-carbonyl]benzonitrile Chemical compound C1(=CC=CC=C1)C(C)(C)NC1=NC=C(C=N1)C(=O)C=1C=C(C#N)C=CC=1 VCAAYIIGVCSPBP-UHFFFAOYSA-N 0.000 claims 1
- RXWGCAHYHQFVJH-UHFFFAOYSA-N 3-[2-(benzylamino)pyrimidine-5-carbonyl]benzonitrile Chemical compound C(C1=CC=CC=C1)NC1=NC=C(C=N1)C(=O)C=1C=C(C#N)C=CC=1 RXWGCAHYHQFVJH-UHFFFAOYSA-N 0.000 claims 1
- FBLFEBHRISBQGZ-UHFFFAOYSA-N 3-[2-(oxan-4-ylmethylamino)pyrimidine-5-carbonyl]benzonitrile Chemical compound O1CCC(CC1)CNC1=NC=C(C=N1)C(=O)C=1C=C(C#N)C=CC=1 FBLFEBHRISBQGZ-UHFFFAOYSA-N 0.000 claims 1
- RQPBVAQLTFXMCV-UHFFFAOYSA-N 3-[2-(pyrazin-2-ylmethylamino)pyrimidine-5-carbonyl]benzonitrile Chemical compound N1=C(C=NC=C1)CNC1=NC=C(C=N1)C(=O)C=1C=C(C#N)C=CC=1 RQPBVAQLTFXMCV-UHFFFAOYSA-N 0.000 claims 1
- MBYRMDHWCNWXMC-UHFFFAOYSA-N 3-[2-(pyridazin-3-ylmethylamino)pyrimidine-5-carbonyl]benzonitrile Chemical compound N1=NC(=CC=C1)CNC1=NC=C(C=N1)C(=O)C=1C=C(C#N)C=CC=1 MBYRMDHWCNWXMC-UHFFFAOYSA-N 0.000 claims 1
- TUIMGCPMHJOPAF-UHFFFAOYSA-N 3-[2-(pyridazin-4-ylmethylamino)pyrimidine-5-carbonyl]benzonitrile Chemical compound N1=NC=C(C=C1)CNC1=NC=C(C=N1)C(=O)C=1C=C(C#N)C=CC=1 TUIMGCPMHJOPAF-UHFFFAOYSA-N 0.000 claims 1
- HHMQWTNSTPXMDJ-UHFFFAOYSA-N 3-[2-(pyrimidin-5-ylmethylamino)pyrimidine-5-carbonyl]benzamide Chemical compound N1=CN=CC(=C1)CNC1=NC=C(C=N1)C(=O)C=1C=C(C(=O)N)C=CC=1 HHMQWTNSTPXMDJ-UHFFFAOYSA-N 0.000 claims 1
- CRPAGROPHFVERB-UHFFFAOYSA-N 3-[2-(pyrimidin-5-ylmethylamino)pyrimidine-5-carbonyl]benzonitrile Chemical compound N1=CN=CC(=C1)CNC1=NC=C(C=N1)C(=O)C=1C=C(C#N)C=CC=1 CRPAGROPHFVERB-UHFFFAOYSA-N 0.000 claims 1
- IPJPYVMHSGTJNY-UHFFFAOYSA-N 3-[2-[(1-methylpiperidin-4-yl)methylamino]pyrimidine-5-carbonyl]benzonitrile Chemical compound CN1CCC(CC1)CNC1=NC=C(C=N1)C(=O)C=1C=C(C#N)C=CC=1 IPJPYVMHSGTJNY-UHFFFAOYSA-N 0.000 claims 1
- AFWPPKALCNDYNE-UHFFFAOYSA-N 3-[2-[(1-phenylcyclobutyl)amino]pyrimidine-5-carbonyl]benzonitrile Chemical compound C1(=CC=CC=C1)C1(CCC1)NC1=NC=C(C=N1)C(=O)C=1C=C(C#N)C=CC=1 AFWPPKALCNDYNE-UHFFFAOYSA-N 0.000 claims 1
- JEKMZYUDLRSXLF-UHFFFAOYSA-N 3-[2-[(1-phenylcyclopropyl)amino]pyrimidine-5-carbonyl]benzonitrile Chemical compound C1(=CC=CC=C1)C1(CC1)NC1=NC=C(C=N1)C(=O)C=1C=C(C#N)C=CC=1 JEKMZYUDLRSXLF-UHFFFAOYSA-N 0.000 claims 1
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- SXGWZYNWYKBEQW-UHFFFAOYSA-N [2-(pyridin-4-ylmethylamino)pyrimidin-5-yl]-[3-(trifluoromethyl)phenyl]methanone Chemical compound N1=CC=C(C=C1)CNC1=NC=C(C=N1)C(=O)C1=CC(=CC=C1)C(F)(F)F SXGWZYNWYKBEQW-UHFFFAOYSA-N 0.000 claims 1
- JJZHBSNPHMHROG-UHFFFAOYSA-N [2-(pyrimidin-5-ylmethylamino)pyrimidin-5-yl]-[2-(trifluoromethyl)pyridin-4-yl]methanone Chemical compound N1=CN=CC(=C1)CNC1=NC=C(C=N1)C(=O)C1=CC(=NC=C1)C(F)(F)F JJZHBSNPHMHROG-UHFFFAOYSA-N 0.000 claims 1
- YXUQMWCGELHLOO-UHFFFAOYSA-N [2-(pyrimidin-5-ylmethylamino)pyrimidin-5-yl]-[3-(trifluoromethyl)phenyl]methanone Chemical compound N1=CN=CC(=C1)CNC1=NC=C(C=N1)C(=O)C1=CC(=CC=C1)C(F)(F)F YXUQMWCGELHLOO-UHFFFAOYSA-N 0.000 claims 1
- XLWPFMGAVDXEOQ-UHFFFAOYSA-N [2-[(1-phenylcyclopropyl)amino]pyrimidin-5-yl]-[3-(trifluoromethyl)phenyl]methanone Chemical compound C1(=CC=CC=C1)C1(CC1)NC1=NC=C(C=N1)C(=O)C1=CC(=CC=C1)C(F)(F)F XLWPFMGAVDXEOQ-UHFFFAOYSA-N 0.000 claims 1
- GNFHKQQNWAUXGW-UHFFFAOYSA-N [2-[(1-pyridin-3-ylcyclopropyl)amino]pyrimidin-5-yl]-[3-(trifluoromethyl)phenyl]methanone Chemical compound N1=CC(=CC=C1)C1(CC1)NC1=NC=C(C=N1)C(=O)C1=CC(=CC=C1)C(F)(F)F GNFHKQQNWAUXGW-UHFFFAOYSA-N 0.000 claims 1
- VUDGJFDRSIQTLT-UHFFFAOYSA-N [2-[(2,4-difluorophenyl)methoxy]pyrimidin-5-yl]-[3-(trifluoromethyl)phenyl]methanone Chemical compound FC1=C(COC2=NC=C(C=N2)C(=O)C2=CC(=CC=C2)C(F)(F)F)C=CC(=C1)F VUDGJFDRSIQTLT-UHFFFAOYSA-N 0.000 claims 1
- XCZWFRIANCZGOF-UHFFFAOYSA-N [2-[(2-fluorophenyl)methylamino]pyrimidin-5-yl]-phenylmethanone Chemical compound FC1=C(CNC2=NC=C(C=N2)C(=O)C2=CC=CC=C2)C=CC=C1 XCZWFRIANCZGOF-UHFFFAOYSA-N 0.000 claims 1
- WGBJVICIIKJPDI-UHFFFAOYSA-N [2-[(4-chloro-2-fluorophenyl)methylamino]pyrimidin-5-yl]-[3-(trifluoromethyl)phenyl]methanone Chemical compound ClC1=CC(=C(CNC2=NC=C(C=N2)C(=O)C2=CC(=CC=C2)C(F)(F)F)C=C1)F WGBJVICIIKJPDI-UHFFFAOYSA-N 0.000 claims 1
- NJQIBJFYXOGCJT-UHFFFAOYSA-N [2-[(4-chlorophenyl)methoxy]pyrimidin-5-yl]-[3-(trifluoromethyl)phenyl]methanone Chemical compound ClC1=CC=C(COC2=NC=C(C=N2)C(=O)C2=CC(=CC=C2)C(F)(F)F)C=C1 NJQIBJFYXOGCJT-UHFFFAOYSA-N 0.000 claims 1
- PINFLIZHILCPDD-UHFFFAOYSA-N [2-[(4-fluorophenyl)methoxy]pyrimidin-5-yl]-[3-(trifluoromethyl)phenyl]methanone Chemical compound FC1=CC=C(COC2=NC=C(C=N2)C(=O)C2=CC(=CC=C2)C(F)(F)F)C=C1 PINFLIZHILCPDD-UHFFFAOYSA-N 0.000 claims 1
- VBHKWOOAFZYOCX-UHFFFAOYSA-N [2-[(4-fluorophenyl)methylamino]pyrimidin-5-yl]-(3-methoxyphenyl)methanone Chemical compound FC1=CC=C(CNC2=NC=C(C=N2)C(=O)C2=CC(=CC=C2)OC)C=C1 VBHKWOOAFZYOCX-UHFFFAOYSA-N 0.000 claims 1
- AOIAZXAIBOFFCK-UHFFFAOYSA-N [2-[(4-fluorophenyl)methylamino]pyrimidin-5-yl]-(3-methylsulfonylphenyl)methanone Chemical compound FC1=CC=C(CNC2=NC=C(C=N2)C(=O)C2=CC(=CC=C2)S(=O)(=O)C)C=C1 AOIAZXAIBOFFCK-UHFFFAOYSA-N 0.000 claims 1
- QVVMWNWZHCZLNC-UHFFFAOYSA-N [2-[(4-fluorophenyl)methylamino]pyrimidin-5-yl]-[3-fluoro-5-(trifluoromethyl)phenyl]methanone Chemical compound FC1=CC=C(CNC2=NC=C(C=N2)C(=O)C2=CC(=CC(=C2)C(F)(F)F)F)C=C1 QVVMWNWZHCZLNC-UHFFFAOYSA-N 0.000 claims 1
- KBWVRCWYQSUQSY-UHFFFAOYSA-N [2-[(4-fluorophenyl)methylamino]pyrimidin-5-yl]-[4-(trifluoromethyl)phenyl]methanone Chemical compound FC1=CC=C(CNC2=NC=C(C=N2)C(=O)C2=CC=C(C=C2)C(F)(F)F)C=C1 KBWVRCWYQSUQSY-UHFFFAOYSA-N 0.000 claims 1
- WOIDWAIDFQIOGK-UHFFFAOYSA-N [2-[(4-fluorophenyl)methylamino]pyrimidin-5-yl]-[4-fluoro-3-(trifluoromethyl)phenyl]methanone Chemical compound FC1=CC=C(CNC2=NC=C(C=N2)C(=O)C2=CC(=C(C=C2)F)C(F)(F)F)C=C1 WOIDWAIDFQIOGK-UHFFFAOYSA-N 0.000 claims 1
- IRVDTYYSNPLUEA-UHFFFAOYSA-N [2-[(4-methoxyphenyl)methoxy]pyrimidin-5-yl]-[3-(trifluoromethyl)phenyl]methanone Chemical compound COC1=CC=C(COC2=NC=C(C=N2)C(=O)C2=CC(=CC=C2)C(F)(F)F)C=C1 IRVDTYYSNPLUEA-UHFFFAOYSA-N 0.000 claims 1
- IFUFEYZEFCQDGE-UHFFFAOYSA-N [2-[(4-methoxyphenyl)methylamino]pyrimidin-5-yl]-[4-(trifluoromethyl)phenyl]methanone Chemical compound COC1=CC=C(CNC2=NC=C(C=N2)C(=O)C2=CC=C(C=C2)C(F)(F)F)C=C1 IFUFEYZEFCQDGE-UHFFFAOYSA-N 0.000 claims 1
- SDRFJZQBHHBCFI-UHFFFAOYSA-N [2-[[4-(trifluoromethoxy)phenyl]methoxy]pyrimidin-5-yl]-[3-(trifluoromethyl)phenyl]methanone Chemical compound FC(OC1=CC=C(COC2=NC=C(C=N2)C(=O)C2=CC(=CC=C2)C(F)(F)F)C=C1)(F)F SDRFJZQBHHBCFI-UHFFFAOYSA-N 0.000 claims 1
- ZFDQTVYRHIFLOP-UHFFFAOYSA-N [2-[[4-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]-[3-(trifluoromethyl)phenyl]methanone Chemical compound FC(OC1=CC=C(CNC2=NC=C(C=N2)C(=O)C2=CC(=CC=C2)C(F)(F)F)C=C1)(F)F ZFDQTVYRHIFLOP-UHFFFAOYSA-N 0.000 claims 1
- IRXNLGLTTUFJNZ-UHFFFAOYSA-N [3-fluoro-5-(trifluoromethyl)phenyl]-[2-(pyridin-3-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound FC=1C=C(C=C(C=1)C(F)(F)F)C(=O)C=1C=NC(=NC=1)NCC=1C=NC=CC=1 IRXNLGLTTUFJNZ-UHFFFAOYSA-N 0.000 claims 1
- OFXOTNYKPLUQRW-UHFFFAOYSA-N [4-fluoro-3-(trifluoromethyl)phenyl]-[2-(pyridin-2-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound FC1=C(C=C(C=C1)C(=O)C=1C=NC(=NC=1)NCC1=NC=CC=C1)C(F)(F)F OFXOTNYKPLUQRW-UHFFFAOYSA-N 0.000 claims 1
- UHFDCKARLZDPRW-UHFFFAOYSA-N [4-fluoro-3-(trifluoromethyl)phenyl]-[2-(pyridin-4-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound FC1=C(C=C(C=C1)C(=O)C=1C=NC(=NC=1)NCC1=CC=NC=C1)C(F)(F)F UHFDCKARLZDPRW-UHFFFAOYSA-N 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000000440 benzylamino group Chemical group [H]N(*)C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 125000004452 carbocyclyl group Chemical group 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 125000002993 cycloalkylene group Chemical group 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims 1
- 230000005764 inhibitory process Effects 0.000 claims 1
- 230000001404 mediated effect Effects 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- ZLVXUGVMIDVPCM-UHFFFAOYSA-N phenyl-[2-(2-phenylpropan-2-ylamino)pyrimidin-5-yl]methanone Chemical compound C1(=CC=CC=C1)C(=O)C=1C=NC(=NC=1)NC(C)(C)C1=CC=CC=C1 ZLVXUGVMIDVPCM-UHFFFAOYSA-N 0.000 claims 1
- NHRXWINZCGSXFX-UHFFFAOYSA-N phenyl-[2-(pyrazin-2-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound C1(=CC=CC=C1)C(=O)C=1C=NC(=NC=1)NCC1=NC=CN=C1 NHRXWINZCGSXFX-UHFFFAOYSA-N 0.000 claims 1
- IBMIDUVNTDPVAD-UHFFFAOYSA-N phenyl-[2-(pyridazin-3-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound C1(=CC=CC=C1)C(=O)C=1C=NC(=NC=1)NCC=1N=NC=CC=1 IBMIDUVNTDPVAD-UHFFFAOYSA-N 0.000 claims 1
- GPZIOKLXQPNWCJ-UHFFFAOYSA-N phenyl-[2-(pyridin-3-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound C1(=CC=CC=C1)C(=O)C=1C=NC(=NC=1)NCC=1C=NC=CC=1 GPZIOKLXQPNWCJ-UHFFFAOYSA-N 0.000 claims 1
- NJQZXBYAOQGCID-UHFFFAOYSA-N phenyl-[2-(pyrimidin-5-ylmethylamino)pyrimidin-5-yl]methanone Chemical compound C1(=CC=CC=C1)C(=O)C=1C=NC(=NC=1)NCC=1C=NC=NC=1 NJQZXBYAOQGCID-UHFFFAOYSA-N 0.000 claims 1
- WLMTYCICQXGBQR-UHFFFAOYSA-N phenyl-[2-[(1-phenylcyclopropyl)amino]pyrimidin-5-yl]methanone Chemical compound C1(=CC=CC=C1)C(=O)C=1C=NC(=NC=1)NC1(CC1)C1=CC=CC=C1 WLMTYCICQXGBQR-UHFFFAOYSA-N 0.000 claims 1
- BRAFADNLUOELAK-UHFFFAOYSA-N phenyl-[2-[(1-pyridin-3-ylcyclopropyl)amino]pyrimidin-5-yl]methanone Chemical compound C1(=CC=CC=C1)C(=O)C=1C=NC(=NC=1)NC1(CC1)C=1C=NC=CC=1 BRAFADNLUOELAK-UHFFFAOYSA-N 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
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| SG11201811161YA (en) * | 2016-07-14 | 2019-01-30 | Pfizer | Novel pyrimidine carboxamides as inhibitors of vanin-1 enzyme |
| EP3824906A1 (en) | 2016-12-21 | 2021-05-26 | Amgen Inc. | Anti-tnf alpha antibody formulations |
| KR101798840B1 (ko) | 2017-05-17 | 2017-11-17 | 주식회사 레고켐 바이오사이언스 | 신규 오토탁신 저해 화합물 및 이를 함유하는 약제학적 조성물 |
| US10961242B2 (en) | 2017-05-17 | 2021-03-30 | Legochem Biosciences, Inc. | Compounds as autotaxin inhibitors and pharmaceutical compositions comprising the same |
| PL3638680T3 (pl) * | 2017-06-12 | 2022-12-19 | Boehringer Ingelheim International Gmbh | Związki heteroaromatyczne jako inhibitory waniny |
| WO2018231702A1 (en) | 2017-06-13 | 2018-12-20 | The Regents Of The University Of California | Methods of improving cell-based therapy |
| US10702488B2 (en) * | 2017-12-19 | 2020-07-07 | Theriac Biomedical Inc. | PPAR-γ activators, HDAC inhibitors and their therapeutical usages |
| US11497723B1 (en) * | 2017-12-19 | 2022-11-15 | Tony Antakly | PPAR-gamma activators, HDAC inhibitors and their therapeutical usages |
| WO2019133445A1 (en) * | 2017-12-28 | 2019-07-04 | Inception Ibd, Inc. | Aminothiazoles as inhibitors of vanin-1 |
| HUE061186T2 (hu) | 2018-08-28 | 2023-06-28 | Boehringer Ingelheim Int | Heteroaromás vegyületek mint vanin-inhibitorok |
| WO2020102575A1 (en) * | 2018-11-16 | 2020-05-22 | Inception Ibd, Inc. | Heterocyclic aminothiazoles and uses thereof |
| CA3116830A1 (en) * | 2018-12-03 | 2020-06-11 | Boehringer Ingelheim International Gmbh | Heteroaromatic compounds as vanin inhibitors |
| CA3120037A1 (en) * | 2018-12-03 | 2020-06-11 | Boehringer Ingelheim International Gmbh | Heteroaromatic compounds as vanin inhibitors |
| BR112021010690A2 (pt) | 2018-12-03 | 2021-08-24 | Boehringer Ingelheim International Gmbh | Compostos heteroaromáticos como inibidores de vanina |
| EP4054556A4 (en) * | 2019-11-07 | 2023-11-29 | Increvet, Inc. | SODIUM-GLUCOSE TRANSPORTER INHIBITORS FOR THE MANAGEMENT OF CHRONIC KIDNEY FAILURE, HYPERTENSION AND HEART FAILURE IN PETS |
| WO2022081716A1 (en) * | 2020-10-13 | 2022-04-21 | Accubit LLC - Biotechnology | Methods of treating iga nephropathy with thiol-containing molecules |
| WO2022127909A1 (zh) * | 2020-12-17 | 2022-06-23 | 上海美悦生物科技发展有限公司 | 一种嘧啶甲酰胺类化合物及其应用 |
| CN120247898A (zh) * | 2025-03-31 | 2025-07-04 | 大连医科大学附属第二医院 | 一种噻吩甲酰胺类化合物及其用途 |
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| US5612359A (en) | 1994-08-26 | 1997-03-18 | Bristol-Myers Squibb Company | Substituted biphenyl isoxazole sulfonamides |
| TW536540B (en) | 1997-01-30 | 2003-06-11 | Bristol Myers Squibb Co | Endothelin antagonists: N-[[2'-[[(4,5-dimethyl-3-isoxazolyl)amino]sulfonyl]-4-(2-oxazolyl)[1,1'-biphenyl]-2-yl]methyl]-N,3,3-trimethylbutanamide and N-(4,5-dimethyl-3-isoxazolyl)-2'-[(3,3-dimethyl-2-oxo-1-pyrrolidinyl)methyl]-4'-(2-oxazolyl)[1,1'-biphe |
| IL140622A0 (en) | 1998-07-06 | 2002-02-10 | Bristol Myers Squibb Co | Biphenyl sufonamide derivatives, pharmaceutical compositions containing the same and methods for the preparation thereof |
| MY125533A (en) | 1999-12-06 | 2006-08-30 | Bristol Myers Squibb Co | Heterocyclic dihydropyrimidine compounds |
| NZ534582A (en) | 2002-02-27 | 2006-03-31 | Pfizer Prod Inc | ACC inhibitors |
| PT1753748E (pt) | 2004-05-12 | 2009-08-28 | Pfizer Prod Inc | Derivados de prolina e a sua utilização como inibidores de dipeptidil peptidase iv |
| ES2487967T3 (es) | 2006-04-20 | 2014-08-25 | Pfizer Products Inc. | Compuestos amido heterocíclicos condensados con fenilo para la prevención y el tratamiento de enfermedades mediadas por la glucoquinasa |
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| CN101541809A (zh) | 2006-11-29 | 2009-09-23 | 辉瑞产品公司 | 螺环酮乙酰基-CoA羧化酶抑制剂 |
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| TW201038580A (en) | 2009-02-02 | 2010-11-01 | Pfizer | 4-amino-5-oxo-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-6(5H)-yl)phenyl derivatives |
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-
2016
- 2016-05-16 EP EP16724127.2A patent/EP3303303A1/en not_active Withdrawn
- 2016-05-16 JP JP2017561653A patent/JP2018516254A/ja active Pending
- 2016-05-16 WO PCT/IB2016/052825 patent/WO2016193844A1/en not_active Ceased
- 2016-05-16 CA CA2987179A patent/CA2987179C/en not_active Expired - Fee Related
- 2016-05-16 US US15/574,625 patent/US10308615B2/en active Active
-
2019
- 2019-04-10 US US16/380,256 patent/US20190292157A1/en not_active Abandoned
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