JP2010540504A5 - - Google Patents
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- Publication number
- JP2010540504A5 JP2010540504A5 JP2010526335A JP2010526335A JP2010540504A5 JP 2010540504 A5 JP2010540504 A5 JP 2010540504A5 JP 2010526335 A JP2010526335 A JP 2010526335A JP 2010526335 A JP2010526335 A JP 2010526335A JP 2010540504 A5 JP2010540504 A5 JP 2010540504A5
- Authority
- JP
- Japan
- Prior art keywords
- pyridin
- phenyl
- ylmethyl
- ureido
- nicotinamide
- 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.)
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- -1 —OH Chemical group 0.000 claims 73
- 150000001875 compounds Chemical class 0.000 claims 44
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 41
- 239000011570 nicotinamide Substances 0.000 claims 34
- 229960003966 nicotinamide Drugs 0.000 claims 34
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 29
- 229910052757 nitrogen Inorganic materials 0.000 claims 20
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 17
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 14
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 13
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 13
- 125000003386 piperidinyl group Chemical group 0.000 claims 11
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 9
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 8
- 125000001072 heteroaryl group Chemical group 0.000 claims 8
- 125000005843 halogen group Chemical group 0.000 claims 7
- 238000000034 method Methods 0.000 claims 7
- 125000004430 oxygen atom Chemical group O* 0.000 claims 7
- 125000004193 piperazinyl group Chemical group 0.000 claims 7
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 7
- 125000003118 aryl group Chemical group 0.000 claims 6
- 239000002253 acid Substances 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 4
- 125000001424 substituent group Chemical group 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 3
- 239000003814 drug Substances 0.000 claims 3
- 229910052731 fluorine Inorganic materials 0.000 claims 3
- 125000001153 fluoro group Chemical group F* 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- 125000002757 morpholinyl group Chemical group 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 125000005988 1,1-dioxo-thiomorpholinyl group Chemical group 0.000 claims 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 125000003725 azepanyl group Chemical group 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
- 125000006239 protecting group Chemical group 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 239000012453 solvate Substances 0.000 claims 2
- 125000004568 thiomorpholinyl group Chemical group 0.000 claims 2
- OSFRJTCATBEZOL-UHFFFAOYSA-N 2-(2-fluoroanilino)-n-(2-piperidin-1-ylethyl)-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound FC1=CC=CC=C1NC1=NC(C=2C=CC(NC(=O)NCC=3C=NC=CC=3)=CC=2)=CC=C1C(=O)NCCN1CCCCC1 OSFRJTCATBEZOL-UHFFFAOYSA-N 0.000 claims 1
- LIXRCDVOCJPBQO-UHFFFAOYSA-N 2-(3-fluoroanilino)-n-(2-piperidin-1-ylethyl)-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound FC1=CC=CC(NC=2C(=CC=C(N=2)C=2C=CC(NC(=O)NCC=3C=NC=CC=3)=CC=2)C(=O)NCCN2CCCCC2)=C1 LIXRCDVOCJPBQO-UHFFFAOYSA-N 0.000 claims 1
- DFMNLKVXICTJRP-UHFFFAOYSA-N 2-(4-fluoroanilino)-n-(2-piperidin-1-ylethyl)-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound C1=CC(F)=CC=C1NC1=NC(C=2C=CC(NC(=O)NCC=3C=NC=CC=3)=CC=2)=CC=C1C(=O)NCCN1CCCCC1 DFMNLKVXICTJRP-UHFFFAOYSA-N 0.000 claims 1
- CLHWNALKFOUJQE-UHFFFAOYSA-N 2-(benzylamino)-n-methyl-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound CNC(=O)C1=CC=C(C=2C=CC(NC(=O)NCC=3C=NC=CC=3)=CC=2)N=C1NCC1=CC=CC=C1 CLHWNALKFOUJQE-UHFFFAOYSA-N 0.000 claims 1
- JZEDQOVFDBGKJN-UHFFFAOYSA-N 2-(ethylamino)-6-[4-[(6-methylpyridin-3-yl)methylcarbamoylamino]phenyl]-n-(2-piperidin-1-ylethyl)pyridine-3-carboxamide Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C=NC(C)=CC=3)=CC=2)=CC=C1C(=O)NCCN1CCCCC1 JZEDQOVFDBGKJN-UHFFFAOYSA-N 0.000 claims 1
- YKEYHLMPWPHUTH-UHFFFAOYSA-N 2-(ethylamino)-6-[4-[[6-(methylamino)pyridin-3-yl]methylcarbamoylamino]phenyl]-n-(2-piperidin-1-ylethyl)pyridine-3-carboxamide Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C=NC(NC)=CC=3)=CC=2)=CC=C1C(=O)NCCN1CCCCC1 YKEYHLMPWPHUTH-UHFFFAOYSA-N 0.000 claims 1
- HVRJRYKKWQFHEJ-UHFFFAOYSA-N 2-(ethylamino)-n-(2-piperazin-1-ylethyl)-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C=NC=CC=3)=CC=2)=CC=C1C(=O)NCCN1CCNCC1 HVRJRYKKWQFHEJ-UHFFFAOYSA-N 0.000 claims 1
- IZNVRNVHWYIXEF-UHFFFAOYSA-N 2-(ethylamino)-n-(2-piperidin-1-ylethyl)-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C=NC=CC=3)=CC=2)=CC=C1C(=O)NCCN1CCCCC1 IZNVRNVHWYIXEF-UHFFFAOYSA-N 0.000 claims 1
- SCJVGQDSOPAGSV-UHFFFAOYSA-N 2-(ethylamino)-n-(2-piperidin-1-ylethyl)-6-[4-[(2,5,6-trifluoropyridin-3-yl)methylcarbamoylamino]phenyl]pyridine-3-carboxamide Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C(=NC(F)=C(F)C=3)F)=CC=2)=CC=C1C(=O)NCCN1CCCCC1 SCJVGQDSOPAGSV-UHFFFAOYSA-N 0.000 claims 1
- FTLVEXPJIRCUQK-UHFFFAOYSA-N 2-(ethylamino)-n-(2-piperidin-1-ylethyl)-6-[4-[[6-(propan-2-ylamino)pyridin-3-yl]methylcarbamoylamino]phenyl]pyridine-3-carboxamide Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C=NC(NC(C)C)=CC=3)=CC=2)=CC=C1C(=O)NCCN1CCCCC1 FTLVEXPJIRCUQK-UHFFFAOYSA-N 0.000 claims 1
- CODQEUJLCKXYLL-UHFFFAOYSA-N 2-(ethylamino)-n-(3-piperidin-1-ylpropyl)-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C=NC=CC=3)=CC=2)=CC=C1C(=O)NCCCN1CCCCC1 CODQEUJLCKXYLL-UHFFFAOYSA-N 0.000 claims 1
- OANBVSVKAQOCFT-UHFFFAOYSA-N 2-(ethylamino)-n-[2-(2-methylpyrrolidin-1-yl)ethyl]-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C=NC=CC=3)=CC=2)=CC=C1C(=O)NCCN1CCCC1C OANBVSVKAQOCFT-UHFFFAOYSA-N 0.000 claims 1
- CTKAJPYTUYQFCT-UHFFFAOYSA-N 2-(ethylamino)-n-[2-(4-hydroxypiperidin-1-yl)ethyl]-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C=NC=CC=3)=CC=2)=CC=C1C(=O)NCCN1CCC(O)CC1 CTKAJPYTUYQFCT-UHFFFAOYSA-N 0.000 claims 1
- BBADFUVNOFFPOQ-UHFFFAOYSA-N 2-(ethylamino)-n-[2-(4-methoxypiperidin-1-yl)ethyl]-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C=NC=CC=3)=CC=2)=CC=C1C(=O)NCCN1CCC(OC)CC1 BBADFUVNOFFPOQ-UHFFFAOYSA-N 0.000 claims 1
- ROVRRAMGHKRPHR-UHFFFAOYSA-N 2-(ethylamino)-n-[2-(4-methylpiperazin-1-yl)ethyl]-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C=NC=CC=3)=CC=2)=CC=C1C(=O)NCCN1CCN(C)CC1 ROVRRAMGHKRPHR-UHFFFAOYSA-N 0.000 claims 1
- URFJUPWAIHGNLG-UHFFFAOYSA-N 2-(ethylamino)-n-[2-(4-propan-2-ylpiperazin-1-yl)ethyl]-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C=NC=CC=3)=CC=2)=CC=C1C(=O)NCCN1CCN(C(C)C)CC1 URFJUPWAIHGNLG-UHFFFAOYSA-N 0.000 claims 1
- AYYCFAAFMVSETP-UHFFFAOYSA-N 2-[2-(dimethylamino)ethylamino]-n-methyl-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound N1=C(NCCN(C)C)C(C(=O)NC)=CC=C1C(C=C1)=CC=C1NC(=O)NCC1=CC=CN=C1 AYYCFAAFMVSETP-UHFFFAOYSA-N 0.000 claims 1
- DCSCUXAXSYPCGL-UHFFFAOYSA-N 2-[4-[(6-aminopyridin-3-yl)methylcarbamoylamino]phenyl]-4-(cyclopropylamino)-n-(2-piperidin-1-ylethyl)pyrimidine-5-carboxamide Chemical compound C1=NC(N)=CC=C1CNC(=O)NC1=CC=C(C=2N=C(NC3CC3)C(C(=O)NCCN3CCCCC3)=CN=2)C=C1 DCSCUXAXSYPCGL-UHFFFAOYSA-N 0.000 claims 1
- SCUYTHNQXMRQCP-UHFFFAOYSA-N 2-anilino-n-(2-piperidin-1-ylethyl)-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound C=1C=C(C=2N=C(NC=3C=CC=CC=3)C(C(=O)NCCN3CCCCC3)=CC=2)C=CC=1NC(=O)NCC1=CC=CN=C1 SCUYTHNQXMRQCP-UHFFFAOYSA-N 0.000 claims 1
- CJNRGSHEMCMUOE-UHFFFAOYSA-N 2-piperidin-1-ylethanamine Chemical compound NCCN1CCCCC1 CJNRGSHEMCMUOE-UHFFFAOYSA-N 0.000 claims 1
- ZNZQZIVPWLLQKN-UHFFFAOYSA-N 2-piperidin-1-ylethyl 2-(ethylamino)-6-[4-[[6-[(2-methylpropan-2-yl)oxycarbonylamino]pyridin-3-yl]methylcarbamoylamino]phenyl]pyridine-3-carboxylate Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C=NC(NC(=O)OC(C)(C)C)=CC=3)=CC=2)=CC=C1C(=O)OCCN1CCCCC1 ZNZQZIVPWLLQKN-UHFFFAOYSA-N 0.000 claims 1
- NXCPGFZOYNHHAU-UHFFFAOYSA-N 4-(ethylamino)-n-methyl-2-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyrimidine-5-carboxamide Chemical compound C1=C(C(=O)NC)C(NCC)=NC(C=2C=CC(NC(=O)NCC=3C=NC=CC=3)=CC=2)=N1 NXCPGFZOYNHHAU-UHFFFAOYSA-N 0.000 claims 1
- QFBWNANOEMPUNO-UHFFFAOYSA-N 6-[4-[(6-amino-5-methylpyridin-3-yl)methylcarbamoylamino]phenyl]-2-(ethylamino)-n-(2-piperidin-1-ylethyl)pyridine-3-carboxamide Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C=C(C)C(N)=NC=3)=CC=2)=CC=C1C(=O)NCCN1CCCCC1 QFBWNANOEMPUNO-UHFFFAOYSA-N 0.000 claims 1
- ZOPCLFRHPBOVBJ-UHFFFAOYSA-N 6-[4-[(6-aminopyridin-3-yl)methylcarbamoylamino]phenyl]-2-(azetidin-1-yl)-n-(2-piperidin-1-ylethyl)pyridine-3-carboxamide Chemical compound C1=NC(N)=CC=C1CNC(=O)NC1=CC=C(C=2N=C(C(C(=O)NCCN3CCCCC3)=CC=2)N2CCC2)C=C1 ZOPCLFRHPBOVBJ-UHFFFAOYSA-N 0.000 claims 1
- LJEMQRNEICXIAC-UHFFFAOYSA-N 6-[4-[(6-aminopyridin-3-yl)methylcarbamoylamino]phenyl]-2-(cyclopropylamino)-n-(2-piperidin-1-ylethyl)pyridine-3-carboxamide Chemical compound C1=NC(N)=CC=C1CNC(=O)NC1=CC=C(C=2N=C(NC3CC3)C(C(=O)NCCN3CCCCC3)=CC=2)C=C1 LJEMQRNEICXIAC-UHFFFAOYSA-N 0.000 claims 1
- PKDBZBMVIIYQGU-UHFFFAOYSA-N 6-[4-[(6-aminopyridin-3-yl)methylcarbamoylamino]phenyl]-2-(ethylamino)-n-(2-hydroxyethyl)pyridine-3-carboxamide Chemical compound C1=C(C(=O)NCCO)C(NCC)=NC(C=2C=CC(NC(=O)NCC=3C=NC(N)=CC=3)=CC=2)=C1 PKDBZBMVIIYQGU-UHFFFAOYSA-N 0.000 claims 1
- YRZJMYJGRFIOIS-UHFFFAOYSA-N 6-[4-[(6-aminopyridin-3-yl)methylcarbamoylamino]phenyl]-2-(ethylamino)-n-(2-methoxyethyl)pyridine-3-carboxamide Chemical compound C1=C(C(=O)NCCOC)C(NCC)=NC(C=2C=CC(NC(=O)NCC=3C=NC(N)=CC=3)=CC=2)=C1 YRZJMYJGRFIOIS-UHFFFAOYSA-N 0.000 claims 1
- JEEVVAUARZJIPJ-UHFFFAOYSA-N 6-[4-[(6-aminopyridin-3-yl)methylcarbamoylamino]phenyl]-2-(ethylamino)-n-(2-morpholin-4-ylethyl)pyridine-3-carboxamide Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C=NC(N)=CC=3)=CC=2)=CC=C1C(=O)NCCN1CCOCC1 JEEVVAUARZJIPJ-UHFFFAOYSA-N 0.000 claims 1
- VEGSKYLXEGANDC-UHFFFAOYSA-N 6-[4-[(6-aminopyridin-3-yl)methylcarbamoylamino]phenyl]-2-(ethylamino)-n-(2-thiomorpholin-4-ylethyl)pyridine-3-carboxamide Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C=NC(N)=CC=3)=CC=2)=CC=C1C(=O)NCCN1CCSCC1 VEGSKYLXEGANDC-UHFFFAOYSA-N 0.000 claims 1
- QVEQVIQBIOCMMP-UHFFFAOYSA-N 6-[4-[(6-aminopyridin-3-yl)methylcarbamoylamino]phenyl]-2-(ethylamino)-n-[2-(1-oxo-1,4-thiazinan-4-yl)ethyl]pyridine-3-carboxamide Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C=NC(N)=CC=3)=CC=2)=CC=C1C(=O)NCCN1CCS(=O)CC1 QVEQVIQBIOCMMP-UHFFFAOYSA-N 0.000 claims 1
- DRSCEJXFSFOGDE-UHFFFAOYSA-N 6-[4-[(6-aminopyridin-3-yl)methylcarbamoylamino]phenyl]-2-(ethylamino)-n-[2-(propan-2-ylamino)ethyl]pyridine-3-carboxamide Chemical compound C1=C(C(=O)NCCNC(C)C)C(NCC)=NC(C=2C=CC(NC(=O)NCC=3C=NC(N)=CC=3)=CC=2)=C1 DRSCEJXFSFOGDE-UHFFFAOYSA-N 0.000 claims 1
- GEFMTLXUJXKRCQ-UHFFFAOYSA-N 6-[4-[(6-aminopyridin-3-yl)methylcarbamoylamino]phenyl]-2-(ethylamino)-n-methylpyridine-3-carboxamide Chemical compound C1=C(C(=O)NC)C(NCC)=NC(C=2C=CC(NC(=O)NCC=3C=NC(N)=CC=3)=CC=2)=C1 GEFMTLXUJXKRCQ-UHFFFAOYSA-N 0.000 claims 1
- KJXMHPNCNGJYKX-UHFFFAOYSA-N 6-[4-[(6-aminopyridin-3-yl)methylcarbamoylamino]phenyl]-2-anilino-n-(2-piperidin-1-ylethyl)pyridine-3-carboxamide Chemical compound C1=NC(N)=CC=C1CNC(=O)NC1=CC=C(C=2N=C(NC=3C=CC=CC=3)C(C(=O)NCCN3CCCCC3)=CC=2)C=C1 KJXMHPNCNGJYKX-UHFFFAOYSA-N 0.000 claims 1
- OPXIKZYDPSQVLW-UHFFFAOYSA-N 6-[4-[(6-aminopyridin-3-yl)methylcarbamoylamino]phenyl]-n-(2-piperidin-1-ylethyl)-2-pyrrolidin-1-ylpyridine-3-carboxamide Chemical compound C1=NC(N)=CC=C1CNC(=O)NC1=CC=C(C=2N=C(C(C(=O)NCCN3CCCCC3)=CC=2)N2CCCC2)C=C1 OPXIKZYDPSQVLW-UHFFFAOYSA-N 0.000 claims 1
- HXMWFJKIKNMKBY-BGYRXZFFSA-N 6-[4-[(6-aminopyridin-3-yl)methylcarbamoylamino]phenyl]-n-[2-[(2s,6r)-2,6-dimethylmorpholin-4-yl]ethyl]-2-(ethylamino)pyridine-3-carboxamide Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C=NC(N)=CC=3)=CC=2)=CC=C1C(=O)NCCN1C[C@H](C)O[C@H](C)C1 HXMWFJKIKNMKBY-BGYRXZFFSA-N 0.000 claims 1
- RFMXBBUTKYRLSO-UHFFFAOYSA-N 6-[4-[(6-aminopyridin-3-yl)methylcarbamoylamino]phenyl]-n-butyl-2-(cyclopropylamino)pyridine-3-carboxamide Chemical compound CCCCNC(=O)C1=CC=C(C=2C=CC(NC(=O)NCC=3C=NC(N)=CC=3)=CC=2)N=C1NC1CC1 RFMXBBUTKYRLSO-UHFFFAOYSA-N 0.000 claims 1
- DAYKKYLISFUMAM-UHFFFAOYSA-N 6-[4-[(6-aminopyridin-3-yl)methylcarbamoylamino]phenyl]-n-cyclopropyl-2-(cyclopropylamino)pyridine-3-carboxamide Chemical compound C1=NC(N)=CC=C1CNC(=O)NC1=CC=C(C=2N=C(NC3CC3)C(C(=O)NC3CC3)=CC=2)C=C1 DAYKKYLISFUMAM-UHFFFAOYSA-N 0.000 claims 1
- JMJDDBCVEKSTEP-UHFFFAOYSA-N 6-[4-[(6-cyanopyridin-3-yl)methylcarbamoylamino]phenyl]-2-(ethylamino)-n-(2-piperidin-1-ylethyl)pyridine-3-carboxamide Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C=NC(=CC=3)C#N)=CC=2)=CC=C1C(=O)NCCN1CCCCC1 JMJDDBCVEKSTEP-UHFFFAOYSA-N 0.000 claims 1
- 239000005973 Carvone Substances 0.000 claims 1
- 241000255925 Diptera Species 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims 1
- 230000003213 activating effect Effects 0.000 claims 1
- 239000012190 activator Substances 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 125000002393 azetidinyl group Chemical group 0.000 claims 1
- BFAKENXZKHGIGE-UHFFFAOYSA-N bis(2,3,5,6-tetrafluoro-4-iodophenyl)diazene Chemical compound FC1=C(C(=C(C(=C1F)I)F)F)N=NC1=C(C(=C(C(=C1F)F)I)F)F BFAKENXZKHGIGE-UHFFFAOYSA-N 0.000 claims 1
- 229910052796 boron Inorganic materials 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 238000010511 deprotection reaction Methods 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- MGJXBDMLVWIYOQ-UHFFFAOYSA-N methylazanide Chemical compound [NH-]C MGJXBDMLVWIYOQ-UHFFFAOYSA-N 0.000 claims 1
- ZBBCSOJFTZPWIS-UHFFFAOYSA-N n-[2-(dimethylamino)ethyl]-2-(ethylamino)-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound C1=C(C(=O)NCCN(C)C)C(NCC)=NC(C=2C=CC(NC(=O)NCC=3C=NC=CC=3)=CC=2)=C1 ZBBCSOJFTZPWIS-UHFFFAOYSA-N 0.000 claims 1
- AEIGFFPISCSEPT-UHFFFAOYSA-N n-[2-[di(propan-2-yl)amino]ethyl]-2-(ethylamino)-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound C1=C(C(=O)NCCN(C(C)C)C(C)C)C(NCC)=NC(C=2C=CC(NC(=O)NCC=3C=NC=CC=3)=CC=2)=C1 AEIGFFPISCSEPT-UHFFFAOYSA-N 0.000 claims 1
- AOMAONSSZDNZFY-CXUHLZMHSA-N n-[2-[di(propan-2-yl)amino]ethyl]-2-(ethylamino)-6-[4-[[(e)-3-pyridin-3-ylprop-2-enoyl]amino]phenyl]pyridine-3-carboxamide Chemical compound C1=C(C(=O)NCCN(C(C)C)C(C)C)C(NCC)=NC(C=2C=CC(NC(=O)\C=C\C=3C=NC=CC=3)=CC=2)=C1 AOMAONSSZDNZFY-CXUHLZMHSA-N 0.000 claims 1
- GRZFIBTYAWGANA-UHFFFAOYSA-N n-methyl-2-(2-piperidin-1-ylethylamino)-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound CNC(=O)C1=CC=C(C=2C=CC(NC(=O)NCC=3C=NC=CC=3)=CC=2)N=C1NCCN1CCCCC1 GRZFIBTYAWGANA-UHFFFAOYSA-N 0.000 claims 1
- UQMNHTJQGHJMHD-UHFFFAOYSA-N n-methyl-2-(propan-2-ylamino)-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound N1=C(NC(C)C)C(C(=O)NC)=CC=C1C(C=C1)=CC=C1NC(=O)NCC1=CC=CN=C1 UQMNHTJQGHJMHD-UHFFFAOYSA-N 0.000 claims 1
- UVQCFCCRNMDDMR-UHFFFAOYSA-N n-methyl-2-(pyridin-2-ylmethylamino)-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound CNC(=O)C1=CC=C(C=2C=CC(NC(=O)NCC=3C=NC=CC=3)=CC=2)N=C1NCC1=CC=CC=N1 UVQCFCCRNMDDMR-UHFFFAOYSA-N 0.000 claims 1
- FAOXRTMFUIVEJY-UHFFFAOYSA-N n-methyl-2-(pyridin-3-ylmethylamino)-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]pyridine-3-carboxamide Chemical compound CNC(=O)C1=CC=C(C=2C=CC(NC(=O)NCC=3C=NC=CC=3)=CC=2)N=C1NCC1=CC=CN=C1 FAOXRTMFUIVEJY-UHFFFAOYSA-N 0.000 claims 1
- XASXCBFMNWFMGU-UHFFFAOYSA-N n-methyl-6-[4-(pyridin-3-ylmethylcarbamoylamino)phenyl]-2-(2-pyrrolidin-1-ylethylamino)pyridine-3-carboxamide Chemical compound CNC(=O)C1=CC=C(C=2C=CC(NC(=O)NCC=3C=NC=CC=3)=CC=2)N=C1NCCN1CCCC1 XASXCBFMNWFMGU-UHFFFAOYSA-N 0.000 claims 1
- 230000003647 oxidation Effects 0.000 claims 1
- 238000007254 oxidation reaction Methods 0.000 claims 1
- 229910052763 palladium Inorganic materials 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
- JWHOQZUREKYPBY-UHFFFAOYSA-N rubonic acid Natural products CC1(C)CCC2(CCC3(C)C(=CCC4C5(C)CCC(=O)C(C)(C)C5CC(=O)C34C)C2C1)C(=O)O JWHOQZUREKYPBY-UHFFFAOYSA-N 0.000 claims 1
- 150000003335 secondary amines Chemical group 0.000 claims 1
- MMISAGDTIIJSFA-UHFFFAOYSA-N tert-butyl n-[5-[[[4-[5-[2-(1,1-dioxo-1,4-thiazinan-4-yl)ethylcarbamoyl]-6-(ethylamino)pyridin-2-yl]phenyl]carbamoylamino]methyl]pyridin-2-yl]carbamate Chemical compound CCNC1=NC(C=2C=CC(NC(=O)NCC=3C=NC(NC(=O)OC(C)(C)C)=CC=3)=CC=2)=CC=C1C(=O)NCCN1CCS(=O)(=O)CC1 MMISAGDTIIJSFA-UHFFFAOYSA-N 0.000 claims 1
- UCPYLLCMEDAXFR-UHFFFAOYSA-N triphosgene Chemical compound ClC(Cl)(Cl)OC(=O)OC(Cl)(Cl)Cl UCPYLLCMEDAXFR-UHFFFAOYSA-N 0.000 claims 1
- 0 *C(c1c(*(*=*)P)nc(-c2ccc(C=C)cc2)nc1)=O Chemical compound *C(c1c(*(*=*)P)nc(-c2ccc(C=C)cc2)nc1)=O 0.000 description 1
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| FR0706799A FR2921657A1 (fr) | 2007-09-28 | 2007-09-28 | Derives de nicotinamide, leur preparation et leur application en therapeutique |
| PCT/FR2008/001338 WO2009074749A2 (fr) | 2007-09-28 | 2008-09-26 | Dérives de nicotinamide. leur préparation et leur application en thérapeutique |
Publications (2)
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| JP2010540504A JP2010540504A (ja) | 2010-12-24 |
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Country Status (19)
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| JP (1) | JP2010540504A (https=) |
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| TW (1) | TW200918056A (https=) |
| UY (1) | UY31367A1 (https=) |
| WO (1) | WO2009074749A2 (https=) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN102775396B (zh) | 2005-11-08 | 2014-10-08 | 沃泰克斯药物股份有限公司 | Atp-结合弹夹转运蛋白的杂环调控剂 |
| CN104447716A (zh) | 2007-05-09 | 2015-03-25 | 沃泰克斯药物股份有限公司 | Cftr调节剂 |
| MX365732B (es) | 2007-12-07 | 2019-06-12 | Vertex Pharma | Procesos para producir acidos cicloalquilcarboxamido-piridin benzoicos. |
| EP3683218B1 (en) | 2007-12-07 | 2024-09-18 | Vertex Pharmaceuticals Incorporated | Solid forms of 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl) cyclopropanecarboxamido)-3-methylpyridin-2-yl) benzoic acid |
| NZ720282A (en) | 2008-02-28 | 2017-12-22 | Vertex Pharma | Heteroaryl derivatives as cftr modulators |
| FR2943675A1 (fr) * | 2009-03-24 | 2010-10-01 | Sanofi Aventis | Composes anticancereux, leur preparation et leur application en therapeutique |
| FR2943670B1 (fr) * | 2009-03-24 | 2011-05-06 | Sanofi Aventis | Derives anticancereux,leur preparation et leur application en therapeutique |
| FR2943669B1 (fr) * | 2009-03-24 | 2011-05-06 | Sanofi Aventis | Derives de nicotinamide,leur preparation et leur application en therapeutique |
| EP2440204B1 (en) * | 2009-06-12 | 2013-12-18 | Bristol-Myers Squibb Company | Nicotinamide compounds useful as kinase modulators |
| AU2011223790A1 (en) * | 2010-03-01 | 2012-08-30 | Myrexis, Inc. | Compounds and therapeutic uses thereof |
| US8912184B1 (en) | 2010-03-01 | 2014-12-16 | Alzheimer's Institute Of America, Inc. | Therapeutic and diagnostic methods |
| JP2013523833A (ja) | 2010-04-07 | 2013-06-17 | バーテックス ファーマシューティカルズ インコーポレイテッド | ３−（６−（１−（２，２−ジフルオロベンゾ［ｄ］［１，３］ジオキソール−５−イル）シクロプロパンカルボキサミド）−３−メチルピリジン−２−イル）安息香酸の医薬組成物およびその投与 |
| US8827372B2 (en) | 2010-07-07 | 2014-09-09 | Frontis Corp. | Blowing system |
| FR2965263A1 (fr) * | 2010-09-24 | 2012-03-30 | Sanofi Aventis | Derives de thienopyridine nicotinamide, leur preparation et leur application en therapeutique |
| US9169246B2 (en) | 2011-09-26 | 2015-10-27 | Sanofi | Pyrazoloquinolinone derivatives, preparation thereof and therapeutic use thereof |
| CN103012397B (zh) * | 2011-09-26 | 2017-03-01 | 赛诺菲 | 吡唑并喹啉酮衍生物、其制备方法及其治疗用途 |
| PT2573073E (pt) * | 2011-09-26 | 2015-02-05 | Sanofi Sa | Derivados de pirazoloquinolinona, sua preparação e sua utilização terapêutica |
| NZ727015A (en) | 2012-01-25 | 2017-12-22 | Vertex Pharma | Formulations of 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl) cyclopropanecarboxamido)-3-methylpyridin-2-yl)benzoic acid |
| AU2014349010C1 (en) | 2013-11-12 | 2020-08-06 | Vertex Pharmaceuticals Incorporated | Process of preparing pharmaceutical compositions for the treatment of CFTR mediated diseases |
| CN103804270B (zh) * | 2014-01-23 | 2016-06-22 | 中国药科大学 | 5-(4-甲脒基苄氧基)色氨酸衍生物、其制法及应用 |
| RU2691136C2 (ru) | 2014-11-18 | 2019-06-11 | Вертекс Фармасьютикалз Инкорпорейтед | Способ проведения высокопроизводительной тестовой высокоэффективной жидкостной хроматографии |
| JP7092356B2 (ja) * | 2016-06-22 | 2022-06-28 | フーダン ユニヴァーシティ | ビアリール尿素誘導体またはそれらの塩、およびそれらの調製方法および使用 |
| CN107522641B (zh) * | 2016-06-22 | 2020-05-05 | 复旦大学 | 联芳基脲类衍生物或其盐及其制备方法和用途 |
| KR102831570B1 (ko) | 2018-05-04 | 2025-07-10 | 레미디 플랜, 인크. | 암 줄기 세포를 표적화하는 암 치료 |
| CN110396065A (zh) * | 2019-06-25 | 2019-11-01 | 南京普锐达医药科技有限公司 | 一种2,4-二氯-5-嘧啶甲酰氯的合成方法 |
| AU2020378067A1 (en) * | 2019-11-06 | 2022-05-26 | Remedy Plan, Inc. | Cancer treatments targeting cancer stem cells |
| WO2021219513A1 (en) | 2020-04-28 | 2021-11-04 | Basf Se | Pesticidal compounds |
| JP2024518089A (ja) * | 2021-05-13 | 2024-04-24 | リメディー プラン，インコーポレーテッド | Ｎａｍｐｔ阻害剤とその使用 |
Family Cites Families (6)
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| DE4301110A1 (de) * | 1993-01-18 | 1994-07-21 | Bayer Ag | Verfahren zur Herstellung von 2-Amino-5-aminomethyl-pyridin |
| CZ20012185A3 (cs) * | 1998-12-16 | 2001-10-17 | Bayer Aktiengesellschaft | Nové bifenylové sloučeniny a sloučeniny analogické bifenylovým sloučeninám, způsob jejich přípravy, farmaceutické prostředky a pouľití těchto sloučenin a prostředků jako antagonistů integrinu |
| DE10063008A1 (de) * | 2000-12-16 | 2002-06-20 | Merck Patent Gmbh | Carbonsäureamidderivate |
| US20040067985A1 (en) * | 2002-10-04 | 2004-04-08 | Fortuna Haviv | Method of inhibiting angiogenesis |
| JP2007515400A (ja) * | 2003-11-28 | 2007-06-14 | ノバルティス アクチエンゲゼルシャフト | タンパク質キナーゼ依存性疾患の処置におけるジアリール尿素誘導体 |
| US20060216288A1 (en) * | 2005-03-22 | 2006-09-28 | Amgen Inc | Combinations for the treatment of cancer |
-
2007
- 2007-09-28 FR FR0706799A patent/FR2921657A1/fr not_active Withdrawn
-
2008
- 2008-09-24 TW TW097136703A patent/TW200918056A/zh unknown
- 2008-09-26 JP JP2010526335A patent/JP2010540504A/ja not_active Withdrawn
- 2008-09-26 KR KR1020107006595A patent/KR20100065165A/ko not_active Withdrawn
- 2008-09-26 EP EP08859496A patent/EP2205566A2/fr not_active Withdrawn
- 2008-09-26 BR BRPI0817973-5A patent/BRPI0817973A2/pt not_active IP Right Cessation
- 2008-09-26 CA CA2700559A patent/CA2700559A1/fr not_active Abandoned
- 2008-09-26 PE PE2008001687A patent/PE20091033A1/es not_active Application Discontinuation
- 2008-09-26 MX MX2010003445A patent/MX2010003445A/es not_active Application Discontinuation
- 2008-09-26 CN CN200880109332A patent/CN101808996A/zh active Pending
- 2008-09-26 CL CL2008002893A patent/CL2008002893A1/es unknown
- 2008-09-26 AU AU2008334457A patent/AU2008334457A1/en not_active Abandoned
- 2008-09-26 UY UY31367A patent/UY31367A1/es not_active Application Discontinuation
- 2008-09-26 RU RU2010116765/04A patent/RU2010116765A/ru not_active Application Discontinuation
- 2008-09-26 PA PA20088797301A patent/PA8797301A1/es unknown
- 2008-09-26 AR ARP080104193A patent/AR066171A1/es unknown
- 2008-09-26 WO PCT/FR2008/001338 patent/WO2009074749A2/fr not_active Ceased
-
2010
- 2010-03-22 IL IL204663A patent/IL204663A0/en unknown
- 2010-03-26 US US12/732,749 patent/US20100222319A1/en not_active Abandoned
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