CA2748099C - 7-phenoxychroman carboxylic acid derivatives - Google Patents
7-phenoxychroman carboxylic acid derivatives Download PDFInfo
- Publication number
- CA2748099C CA2748099C CA2748099A CA2748099A CA2748099C CA 2748099 C CA2748099 C CA 2748099C CA 2748099 A CA2748099 A CA 2748099A CA 2748099 A CA2748099 A CA 2748099A CA 2748099 C CA2748099 C CA 2748099C
- Authority
- CA
- Canada
- Prior art keywords
- phenoxy
- carboxylic acid
- chroman
- ylcarbamoyl
- chloro
- 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.)
- Expired - Fee Related
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- XLFDDXZOBBEBLN-UHFFFAOYSA-N 7-phenoxy-3,4-dihydro-2h-chromene-2-carboxylic acid Chemical class C1=C2OC(C(=O)O)CCC2=CC=C1OC1=CC=CC=C1 XLFDDXZOBBEBLN-UHFFFAOYSA-N 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims abstract description 270
- 238000011282 treatment Methods 0.000 claims abstract description 16
- 238000004519 manufacturing process Methods 0.000 claims abstract description 6
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 115
- -1 2-oxopyridin-1(2H)-yl Chemical group 0.000 claims description 106
- 125000000217 alkyl group Chemical group 0.000 claims description 86
- 125000001424 substituent group Chemical group 0.000 claims description 68
- RGWHTTALQBHDGZ-UHFFFAOYSA-N 3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound C1=CC=C2C(C(=O)O)CCOC2=C1 RGWHTTALQBHDGZ-UHFFFAOYSA-N 0.000 claims description 64
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 60
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 49
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 45
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 39
- 229910052736 halogen Inorganic materials 0.000 claims description 37
- 150000002367 halogens Chemical class 0.000 claims description 37
- 229910052739 hydrogen Inorganic materials 0.000 claims description 34
- 159000000000 sodium salts Chemical group 0.000 claims description 33
- 125000005842 heteroatom Chemical group 0.000 claims description 32
- 150000003839 salts Chemical class 0.000 claims description 28
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 26
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 25
- 125000004429 atom Chemical group 0.000 claims description 23
- 229910052801 chlorine Inorganic materials 0.000 claims description 22
- 239000003446 ligand Substances 0.000 claims description 22
- GWDVHHFYMYWYNA-UHFFFAOYSA-N 6-chloro-7-[4-[[6-(4-chlorophenyl)pyridin-2-yl]carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NC(N=1)=CC=CC=1C1=CC=C(Cl)C=C1 GWDVHHFYMYWYNA-UHFFFAOYSA-N 0.000 claims description 21
- 125000001072 heteroaryl group Chemical group 0.000 claims description 21
- YYASZOUWMTWJBY-UHFFFAOYSA-N 6-chloro-7-[4-[(6-chloroquinolin-2-yl)carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound C1=C(Cl)C=CC2=NC(NC(=O)C3=CC=C(C=C3)OC=3C=C4OCCC(C4=CC=3Cl)C(=O)O)=CC=C21 YYASZOUWMTWJBY-UHFFFAOYSA-N 0.000 claims description 20
- 239000003054 catalyst Substances 0.000 claims description 20
- 229910052731 fluorine Inorganic materials 0.000 claims description 20
- 125000006163 5-membered heteroaryl group Chemical group 0.000 claims description 17
- 230000008878 coupling Effects 0.000 claims description 17
- 238000010168 coupling process Methods 0.000 claims description 17
- 238000005859 coupling reaction Methods 0.000 claims description 17
- 125000006575 electron-withdrawing group Chemical group 0.000 claims description 16
- 239000001257 hydrogen Substances 0.000 claims description 16
- 229910052794 bromium Inorganic materials 0.000 claims description 14
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 14
- 241000124008 Mammalia Species 0.000 claims description 12
- 229910052763 palladium Inorganic materials 0.000 claims description 12
- 125000006239 protecting group Chemical group 0.000 claims description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
- WLVKDFJTYKELLQ-UHFFFAOYSA-N cyclopropylboronic acid Chemical compound OB(O)C1CC1 WLVKDFJTYKELLQ-UHFFFAOYSA-N 0.000 claims description 10
- 125000004076 pyridyl group Chemical group 0.000 claims description 10
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 9
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- HRBZUZZOAMLGEA-UHFFFAOYSA-N 6-chloro-7-[4-[(8-methylquinolin-2-yl)carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound O1CCC(C(O)=O)C(C=C2Cl)=C1C=C2OC(C=C1)=CC=C1C(=O)NC1=CC=C2C=CC=C(C)C2=N1 HRBZUZZOAMLGEA-UHFFFAOYSA-N 0.000 claims description 7
- OWMWSDWNPGDQAO-UHFFFAOYSA-N 6-chloro-7-[4-[2-[6-cyclopropyl-2-(dimethylamino)pyridin-3-yl]ethylcarbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound C=1C=C(CCNC(=O)C=2C=CC(OC=3C(=CC=4C(C(O)=O)CCOC=4C=3)Cl)=CC=2)C(N(C)C)=NC=1C1CC1 OWMWSDWNPGDQAO-UHFFFAOYSA-N 0.000 claims description 7
- SJHMZSZLEVAPPS-UHFFFAOYSA-N 6-chloro-7-[4-[(4-methylquinolin-2-yl)carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound C1=CC=C2C(C)=CC(NC(=O)C=3C=CC(OC=4C(=CC=5C(C(O)=O)CCOC=5C=4)Cl)=CC=3)=NC2=C1 SJHMZSZLEVAPPS-UHFFFAOYSA-N 0.000 claims description 6
- XNYIKJKWMIPXIC-UHFFFAOYSA-N 6-chloro-7-[4-[(5-chloroquinolin-2-yl)carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC1=CC=CC2=NC(NC(=O)C3=CC=C(C=C3)OC=3C=C4OCCC(C4=CC=3Cl)C(=O)O)=CC=C21 XNYIKJKWMIPXIC-UHFFFAOYSA-N 0.000 claims description 6
- FZHBLVWFBLYBRU-UHFFFAOYSA-N 6-chloro-7-[4-[(6-phenylpyrazin-2-yl)carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NC(N=1)=CN=CC=1C1=CC=CC=C1 FZHBLVWFBLYBRU-UHFFFAOYSA-N 0.000 claims description 6
- AAMHDHWZSLVHKR-UHFFFAOYSA-N 6-chloro-7-[4-[[6-[4-(trifluoromethyl)phenyl]pyridazin-3-yl]carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NC(N=N1)=CC=C1C1=CC=C(C(F)(F)F)C=C1 AAMHDHWZSLVHKR-UHFFFAOYSA-N 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 239000003814 drug Substances 0.000 claims description 6
- NYLDFERJNDCQBO-UHFFFAOYSA-N 6-chloro-7-[4-[2-(6-cyclopropyl-2-methoxypyridin-3-yl)ethylcarbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound C=1C=C(CCNC(=O)C=2C=CC(OC=3C(=CC=4C(C(O)=O)CCOC=4C=3)Cl)=CC=2)C(OC)=NC=1C1CC1 NYLDFERJNDCQBO-UHFFFAOYSA-N 0.000 claims description 5
- YNHGPRVRAXSUMU-UHFFFAOYSA-N 6-chloro-7-[4-[2-[2-cyclopropyl-6-(trifluoromethyl)pyridin-3-yl]ethylcarbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NCCC1=CC=C(C(F)(F)F)N=C1C1CC1 YNHGPRVRAXSUMU-UHFFFAOYSA-N 0.000 claims description 5
- BZSIIAXZXXYBNG-UHFFFAOYSA-N 6-cyano-7-[4-(quinolin-3-ylcarbamoyl)phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound C1=CC=CC2=CC(NC(=O)C3=CC=C(C=C3)OC=3C=C4OCCC(C4=CC=3C#N)C(=O)O)=CN=C21 BZSIIAXZXXYBNG-UHFFFAOYSA-N 0.000 claims description 5
- VKTOBDTYSOSXNN-UHFFFAOYSA-N 7-[4-[[5-(4-chlorophenyl)-1,3,4-thiadiazol-2-yl]carbamoyl]phenoxy]-6-cyano-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound N#CC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NC(S1)=NN=C1C1=CC=C(Cl)C=C1 VKTOBDTYSOSXNN-UHFFFAOYSA-N 0.000 claims description 5
- 150000001879 copper Chemical class 0.000 claims description 5
- OPGLODHIMZZHOF-UHFFFAOYSA-N 6-chloro-7-[4-[(6-ethoxypyridin-2-yl)carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound CCOC1=CC=CC(NC(=O)C=2C=CC(OC=3C(=CC=4C(C(O)=O)CCOC=4C=3)Cl)=CC=2)=N1 OPGLODHIMZZHOF-UHFFFAOYSA-N 0.000 claims description 4
- ZYBBRMMZDJYIPW-UHFFFAOYSA-N 6-chloro-7-[4-[(6-phenylpyridin-2-yl)carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NC(N=1)=CC=CC=1C1=CC=CC=C1 ZYBBRMMZDJYIPW-UHFFFAOYSA-N 0.000 claims description 4
- OUYSBENYJUSRMS-UHFFFAOYSA-N 6-chloro-7-[4-[2-(3,5-dichloropyridin-2-yl)ethylcarbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NCCC1=NC=C(Cl)C=C1Cl OUYSBENYJUSRMS-UHFFFAOYSA-N 0.000 claims description 4
- ARYZFRWMNCQJDZ-UHFFFAOYSA-N 6-chloro-7-[4-[2-[2-methoxy-6-(trifluoromethyl)pyridin-3-yl]ethylcarbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound COC1=NC(C(F)(F)F)=CC=C1CCNC(=O)C(C=C1)=CC=C1OC(C(=C1)Cl)=CC2=C1C(C(O)=O)CCO2 ARYZFRWMNCQJDZ-UHFFFAOYSA-N 0.000 claims description 4
- QMZNCJJCBUYPHV-UHFFFAOYSA-N 6-chloro-7-[4-[[1-(3,4-difluorophenyl)pyrazol-3-yl]carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NC(=N1)C=CN1C1=CC=C(F)C(F)=C1 QMZNCJJCBUYPHV-UHFFFAOYSA-N 0.000 claims description 4
- FRRRYBLSANIYRN-UHFFFAOYSA-N 6-chloro-7-[4-[[1-(3-chlorophenyl)pyrazol-4-yl]carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NC(=C1)C=NN1C1=CC=CC(Cl)=C1 FRRRYBLSANIYRN-UHFFFAOYSA-N 0.000 claims description 4
- DIYOYANZNFBPIV-UHFFFAOYSA-N 6-chloro-7-[4-[[2-(3-chlorophenyl)pyrimidin-5-yl]carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NC(C=N1)=CN=C1C1=CC=CC(Cl)=C1 DIYOYANZNFBPIV-UHFFFAOYSA-N 0.000 claims description 4
- SPINOQDNCUSTKB-UHFFFAOYSA-N 6-chloro-7-[4-[[4-[4-(trifluoromethyl)phenyl]pyrimidin-2-yl]carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NC(N=1)=NC=CC=1C1=CC=C(C(F)(F)F)C=C1 SPINOQDNCUSTKB-UHFFFAOYSA-N 0.000 claims description 4
- ZHDLHVSCMVNSPV-UHFFFAOYSA-N 6-chloro-7-[4-[[5-(4-chlorophenyl)pyridin-2-yl]carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NC(N=C1)=CC=C1C1=CC=C(Cl)C=C1 ZHDLHVSCMVNSPV-UHFFFAOYSA-N 0.000 claims description 4
- DZEPISVCRQTZFC-UHFFFAOYSA-N 6-chloro-7-[4-[[6-(3,4-dichlorophenyl)pyridin-2-yl]carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NC(N=1)=CC=CC=1C1=CC=C(Cl)C(Cl)=C1 DZEPISVCRQTZFC-UHFFFAOYSA-N 0.000 claims description 4
- JHGPUDIYXDMHKJ-UHFFFAOYSA-N 6-chloro-7-[4-[[6-(3-chlorophenyl)pyrazin-2-yl]carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NC(N=1)=CN=CC=1C1=CC=CC(Cl)=C1 JHGPUDIYXDMHKJ-UHFFFAOYSA-N 0.000 claims description 4
- HYHJMSJZZBYJBZ-UHFFFAOYSA-N 6-chloro-7-[4-[[6-(4-chlorophenyl)-5-fluoropyridin-2-yl]carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NC(N=1)=CC=C(F)C=1C1=CC=C(Cl)C=C1 HYHJMSJZZBYJBZ-UHFFFAOYSA-N 0.000 claims description 4
- OQPQBEQBVTVBCQ-UHFFFAOYSA-N 6-chloro-7-[4-[[6-(4-methylphenyl)pyridin-2-yl]carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound C1=CC(C)=CC=C1C1=CC=CC(NC(=O)C=2C=CC(OC=3C(=CC=4C(C(O)=O)CCOC=4C=3)Cl)=CC=2)=N1 OQPQBEQBVTVBCQ-UHFFFAOYSA-N 0.000 claims description 4
- NPQGSVSVVBMWIH-UHFFFAOYSA-N 6-chloro-7-[4-[[6-[2-chloro-4-(trifluoromethyl)phenyl]pyridazin-3-yl]carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NC(N=N1)=CC=C1C1=CC=C(C(F)(F)F)C=C1Cl NPQGSVSVVBMWIH-UHFFFAOYSA-N 0.000 claims description 4
- JRTKPZRXXAFERK-UHFFFAOYSA-N 6-chloro-7-[4-[[6-[2-fluoro-4-(trifluoromethyl)phenyl]pyridazin-3-yl]carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NC(N=N1)=CC=C1C1=CC=C(C(F)(F)F)C=C1F JRTKPZRXXAFERK-UHFFFAOYSA-N 0.000 claims description 4
- HDWHDDUVTFWFTG-UHFFFAOYSA-N 6-cyano-7-[4-[(5-phenyl-1,3,4-thiadiazol-2-yl)carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound N#CC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NC(S1)=NN=C1C1=CC=CC=C1 HDWHDDUVTFWFTG-UHFFFAOYSA-N 0.000 claims description 4
- OTCZFDOCIXJFBU-UHFFFAOYSA-N 6-cyano-7-[4-[2-[5-(trifluoromethyl)pyridin-2-yl]ethylcarbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound N#CC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NCCC1=CC=C(C(F)(F)F)C=N1 OTCZFDOCIXJFBU-UHFFFAOYSA-N 0.000 claims description 4
- GZXFDSKBZKZYTR-UHFFFAOYSA-N 6-cyano-7-[4-[[5-(trifluoromethyl)pyridin-2-yl]carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound N#CC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NC1=CC=C(C(F)(F)F)C=N1 GZXFDSKBZKZYTR-UHFFFAOYSA-N 0.000 claims description 4
- DZQHRTYQJRHWQE-UHFFFAOYSA-N 6-cyano-7-[4-[[6-(3,4-dimethylphenyl)pyridin-2-yl]carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound C1=C(C)C(C)=CC=C1C1=CC=CC(NC(=O)C=2C=CC(OC=3C(=CC=4C(C(O)=O)CCOC=4C=3)C#N)=CC=2)=N1 DZQHRTYQJRHWQE-UHFFFAOYSA-N 0.000 claims description 4
- YLYOKCKVFUCCCK-UHFFFAOYSA-N 6-cyano-7-[4-[[6-(trifluoromethyl)pyridin-3-yl]carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound N#CC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NC1=CC=C(C(F)(F)F)N=C1 YLYOKCKVFUCCCK-UHFFFAOYSA-N 0.000 claims description 4
- VVVLCEWRMAEEIH-UHFFFAOYSA-N 7-[4-[(4-tert-butyl-1,3-thiazol-2-yl)carbamoyl]phenoxy]-6-chloro-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound CC(C)(C)C1=CSC(NC(=O)C=2C=CC(OC=3C(=CC=4C(C(O)=O)CCOC=4C=3)Cl)=CC=2)=N1 VVVLCEWRMAEEIH-UHFFFAOYSA-N 0.000 claims description 4
- ISVMYAIYXBBHRC-UHFFFAOYSA-N 7-[4-[(6-tert-butylpyridin-2-yl)carbamoyl]phenoxy]-6-chloro-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound CC(C)(C)C1=CC=CC(NC(=O)C=2C=CC(OC=3C(=CC=4C(C(O)=O)CCOC=4C=3)Cl)=CC=2)=N1 ISVMYAIYXBBHRC-UHFFFAOYSA-N 0.000 claims description 4
- 230000001900 immune effect Effects 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 239000008194 pharmaceutical composition Substances 0.000 claims description 4
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- FCMCTZXRSOYHAJ-UHFFFAOYSA-N 6,8-dichloro-7-[4-[[6-(3-chlorophenyl)pyridin-3-yl]carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC=1C=C2C(C(=O)O)CCOC2=C(Cl)C=1OC(C=C1)=CC=C1C(=O)NC(C=N1)=CC=C1C1=CC=CC(Cl)=C1 FCMCTZXRSOYHAJ-UHFFFAOYSA-N 0.000 claims description 3
- ODEXLFJUFJNFGN-UHFFFAOYSA-N 6,8-dichloro-7-[4-[[6-(4-chlorophenyl)pyridin-2-yl]carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC=1C=C2C(C(=O)O)CCOC2=C(Cl)C=1OC(C=C1)=CC=C1C(=O)NC(N=1)=CC=CC=1C1=CC=C(Cl)C=C1 ODEXLFJUFJNFGN-UHFFFAOYSA-N 0.000 claims description 3
- RFQWZVDCGCJUNL-UHFFFAOYSA-N 6-chloro-7-[4-(quinolin-2-ylcarbamoyl)phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound C1=CC=CC2=NC(NC(=O)C3=CC=C(C=C3)OC=3C=C4OCCC(C4=CC=3Cl)C(=O)O)=CC=C21 RFQWZVDCGCJUNL-UHFFFAOYSA-N 0.000 claims description 3
- INWQZPNIGBKAIH-UHFFFAOYSA-N 6-chloro-7-[4-[(3-methylquinolin-2-yl)carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound O1CCC(C(O)=O)C(C=C2Cl)=C1C=C2OC(C=C1)=CC=C1C(=O)NC1=NC2=CC=CC=C2C=C1C INWQZPNIGBKAIH-UHFFFAOYSA-N 0.000 claims description 3
- FQRDDNOFDCFIBV-UHFFFAOYSA-N 6-chloro-7-[4-[(5-phenyl-1,3,4-thiadiazol-2-yl)carbamoyl]phenoxy]-3,4-dihydro-2h-chromene-4-carboxylic acid Chemical compound ClC=1C=C2C(C(=O)O)CCOC2=CC=1OC(C=C1)=CC=C1C(=O)NC(S1)=NN=C1C1=CC=CC=C1 FQRDDNOFDCFIBV-UHFFFAOYSA-N 0.000 claims description 3
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Classifications
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- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
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- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Ophthalmology & Optometry (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Otolaryngology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13998108P | 2008-12-22 | 2008-12-22 | |
| US61/139,981 | 2008-12-22 | ||
| PCT/US2009/068672 WO2010075200A1 (en) | 2008-12-22 | 2009-12-18 | 7-phenoxychroman carboxylic acid derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2748099A1 CA2748099A1 (en) | 2010-07-01 |
| CA2748099C true CA2748099C (en) | 2017-02-28 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2748099A Expired - Fee Related CA2748099C (en) | 2008-12-22 | 2009-12-18 | 7-phenoxychroman carboxylic acid derivatives |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US8785445B2 (enExample) |
| EP (1) | EP2379535B1 (enExample) |
| JP (1) | JP5575799B2 (enExample) |
| CN (1) | CN102325767B (enExample) |
| CA (1) | CA2748099C (enExample) |
| TW (1) | TWI469977B (enExample) |
| WO (1) | WO2010075200A1 (enExample) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2582161T3 (es) * | 2008-06-25 | 2016-09-09 | Array Biopharma, Inc. | Derivados del ácido fenoxicroman carboxílico sustituidos en 6 |
| EP2376485B1 (en) | 2008-12-19 | 2017-12-06 | Vertex Pharmaceuticals Incorporated | Pyrazine derivatives useful as inhibitors of atr kinase |
| JP2013526540A (ja) * | 2010-05-12 | 2013-06-24 | 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 | Atrキナーゼ阻害剤として有用な化合物 |
| KR20130066633A (ko) | 2010-05-12 | 2013-06-20 | 버텍스 파마슈티칼스 인코포레이티드 | Atr 키나제의 억제제로서 유용한 화합물 |
| BR112014007690B1 (pt) | 2011-09-30 | 2022-10-04 | Vertex Pharmaceuticals Incorporated | Usos de inibidores de atr no tratamento de câncer pancreático e câncer de pulmão de células não pequenas |
| CN103987709B (zh) | 2011-09-30 | 2016-09-28 | 沃泰克斯药物股份有限公司 | 用于制备可用作atr激酶抑制剂的化合物的方法 |
| EP3311816A1 (en) | 2012-04-05 | 2018-04-25 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase for the treatment of cancer |
| CA2873097A1 (en) | 2012-05-11 | 2013-11-14 | Todd M. Hansen | Pyridazine and pyridine derivatives as nampt inhibitors |
| TWI654180B (zh) | 2012-06-29 | 2019-03-21 | 美商艾佛艾姆希公司 | 殺真菌之雜環羧醯胺 |
| US8999632B2 (en) | 2012-10-04 | 2015-04-07 | Vertex Pharmaceuticals Incorporated | Method for measuring ATR inhibition mediated increases in DNA damage |
| EP4420734A3 (en) * | 2015-02-13 | 2024-11-06 | Institut National de la Santé et de la Recherche Médicale | Ptgdr-1 and/or ptgdr-2 antagonists for preventing and/or treating systemic lupus erythematosus |
| RU2768621C1 (ru) | 2015-09-30 | 2022-03-24 | Вертекс Фармасьютикалз Инкорпорейтед | Способ лечения рака с использованием комбинации повреждающих днк средств и ингибиторов atr |
| WO2021063735A1 (en) | 2019-10-02 | 2021-04-08 | Basf Se | New bicyclic pyridine derivatives |
| CN111228247B (zh) * | 2019-12-05 | 2023-01-31 | 青海大学 | 一种用于治疗包虫病的含苯亚甲基丙酮药物及其制备方法 |
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| US20070119975A1 (en) * | 2001-11-28 | 2007-05-31 | Hunnicutt S B | Method and Apparatus for Reducing the Precipitation Rate of an Irrigation Sprinkler |
| CA2511214C (en) * | 2002-12-20 | 2012-12-18 | Tularik, Inc. | Asthma and allergic inflammation modulators |
| GB0611781D0 (en) | 2006-06-14 | 2006-07-26 | Argenta Discovery Ltd | 2-Oxo-2H-Chromene Compounds |
| HRP20130004T8 (en) * | 2006-08-21 | 2013-03-31 | Array Biopharma, Inc. | 4-substituted phenoxyphenylacetic acid derivatives |
| WO2008054675A2 (en) | 2006-10-31 | 2008-05-08 | Merck & Co., Inc. | Antidiabetic bicyclic compounds |
| US7960567B2 (en) * | 2007-05-02 | 2011-06-14 | Amgen Inc. | Compounds and methods useful for treating asthma and allergic inflammation |
| US8362056B2 (en) | 2007-11-05 | 2013-01-29 | Array Biopharma Inc. | 4-heteroaryl-substituted phenoxyphenylacetic acid derivatives |
| ES2582161T3 (es) * | 2008-06-25 | 2016-09-09 | Array Biopharma, Inc. | Derivados del ácido fenoxicroman carboxílico sustituidos en 6 |
-
2009
- 2009-12-18 US US13/141,675 patent/US8785445B2/en not_active Expired - Fee Related
- 2009-12-18 CA CA2748099A patent/CA2748099C/en not_active Expired - Fee Related
- 2009-12-18 WO PCT/US2009/068672 patent/WO2010075200A1/en not_active Ceased
- 2009-12-18 CN CN200980157228.9A patent/CN102325767B/zh not_active Expired - Fee Related
- 2009-12-18 EP EP09793682.7A patent/EP2379535B1/en active Active
- 2009-12-18 JP JP2011542470A patent/JP5575799B2/ja not_active Expired - Fee Related
- 2009-12-22 TW TW98144271A patent/TWI469977B/zh not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| US20120101103A1 (en) | 2012-04-26 |
| JP2012513398A (ja) | 2012-06-14 |
| WO2010075200A1 (en) | 2010-07-01 |
| CN102325767B (zh) | 2014-05-14 |
| TW201028402A (en) | 2010-08-01 |
| US8785445B2 (en) | 2014-07-22 |
| TWI469977B (zh) | 2015-01-21 |
| CN102325767A (zh) | 2012-01-18 |
| JP5575799B2 (ja) | 2014-08-20 |
| CA2748099A1 (en) | 2010-07-01 |
| EP2379535B1 (en) | 2016-06-15 |
| EP2379535A1 (en) | 2011-10-26 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request |
Effective date: 20141128 |
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| MKLA | Lapsed |
Effective date: 20211220 |