JP2010513334A5 - - Google Patents
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- Publication number
- JP2010513334A5 JP2010513334A5 JP2009541766A JP2009541766A JP2010513334A5 JP 2010513334 A5 JP2010513334 A5 JP 2010513334A5 JP 2009541766 A JP2009541766 A JP 2009541766A JP 2009541766 A JP2009541766 A JP 2009541766A JP 2010513334 A5 JP2010513334 A5 JP 2010513334A5
- Authority
- JP
- Japan
- Prior art keywords
- compound
- pyridin
- dichloro
- dimethoxy
- phenyl
- 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.)
- Granted
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- 150000001875 compounds Chemical class 0.000 claims 207
- -1 hydrate Chemical class 0.000 claims 71
- 239000001257 hydrogen Substances 0.000 claims 37
- 229910052739 hydrogen Inorganic materials 0.000 claims 37
- 125000001424 substituent group Chemical group 0.000 claims 28
- 125000000217 alkyl group Chemical group 0.000 claims 26
- 150000002431 hydrogen Chemical class 0.000 claims 25
- 125000001188 haloalkyl group Chemical group 0.000 claims 22
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 21
- 125000003342 alkenyl group Chemical group 0.000 claims 18
- 125000000304 alkynyl group Chemical group 0.000 claims 18
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 18
- 125000003545 alkoxy group Chemical group 0.000 claims 17
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 17
- 125000004043 oxo group Chemical group O=* 0.000 claims 17
- 125000000753 cycloalkyl group Chemical group 0.000 claims 16
- 229910052736 halogen Inorganic materials 0.000 claims 15
- 150000002367 halogens Chemical class 0.000 claims 15
- 125000003118 aryl group Chemical group 0.000 claims 14
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 12
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 12
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 12
- 125000004104 aryloxy group Chemical group 0.000 claims 11
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 11
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 10
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 10
- 125000002877 alkyl aryl group Chemical group 0.000 claims 10
- 125000004414 alkyl thio group Chemical group 0.000 claims 10
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 10
- 125000004093 cyano group Chemical group *C#N 0.000 claims 9
- 201000004624 Dermatitis Diseases 0.000 claims 8
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 8
- 125000004366 heterocycloalkenyl group Chemical group 0.000 claims 8
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims 7
- 125000003710 aryl alkyl group Chemical group 0.000 claims 7
- 239000008194 pharmaceutical composition Substances 0.000 claims 7
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 6
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 claims 6
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims 6
- 125000005129 aryl carbonyl group Chemical group 0.000 claims 6
- 125000000623 heterocyclic group Chemical group 0.000 claims 6
- 125000001153 fluoro group Chemical group F* 0.000 claims 5
- 125000001072 heteroaryl group Chemical group 0.000 claims 5
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 5
- ODLMAHJVESYWTB-UHFFFAOYSA-N propylbenzene Chemical compound CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 claims 5
- 208000017520 skin disease Diseases 0.000 claims 5
- XNMQEEKYCVKGBD-UHFFFAOYSA-N 2-butyne Chemical compound CC#CC XNMQEEKYCVKGBD-UHFFFAOYSA-N 0.000 claims 4
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims 4
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 claims 4
- 206010040799 Skin atrophy Diseases 0.000 claims 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 4
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 claims 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims 4
- 125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 claims 4
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 4
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 3
- 150000001204 N-oxides Chemical class 0.000 claims 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Substances N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims 3
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 claims 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 3
- 150000002148 esters Chemical class 0.000 claims 3
- 125000004076 pyridyl group Chemical group 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 239000012453 solvate Substances 0.000 claims 3
- 208000024891 symptom Diseases 0.000 claims 3
- 125000003944 tolyl group Chemical group 0.000 claims 3
- JMSLXMMWELRQMU-UHFFFAOYSA-N 1-(2-but-2-ynoxy-3,4-dimethoxyphenyl)-2-(3,5-dichloropyridin-4-yl)ethanone Chemical compound CC#CCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl JMSLXMMWELRQMU-UHFFFAOYSA-N 0.000 claims 2
- GMRZCWUZXHCTOJ-UHFFFAOYSA-N 1-(2-but-3-enoxy-3,4-dimethoxyphenyl)-2-(3,5-dichloropyridin-4-yl)ethanone Chemical compound C=CCCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl GMRZCWUZXHCTOJ-UHFFFAOYSA-N 0.000 claims 2
- IAWADUJZYLNTIM-UHFFFAOYSA-N 1-(2-butoxy-3,4-dimethoxyphenyl)-2-(3,5-dichloropyridin-4-yl)ethanone Chemical compound C1=CC(OC)=C(OC)C(OCCCC)=C1C(=O)CC1=C(Cl)C=NC=C1Cl IAWADUJZYLNTIM-UHFFFAOYSA-N 0.000 claims 2
- NFUFDHIMMGDBHD-UHFFFAOYSA-N 1-(3-but-2-ynoxy-2,4-dimethoxyphenyl)-2-(3,5-dichloropyridin-4-yl)ethanone Chemical compound COC1=C(OCC#CC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl NFUFDHIMMGDBHD-UHFFFAOYSA-N 0.000 claims 2
- DOLXLIULMTUVPH-UHFFFAOYSA-N 1-(3-but-3-enoxy-2,4-dimethoxyphenyl)-2-(3,5-dichloropyridin-4-yl)ethanone Chemical compound COC1=C(OCCC=C)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl DOLXLIULMTUVPH-UHFFFAOYSA-N 0.000 claims 2
- OXLLLXVNJUIDJX-UHFFFAOYSA-N 1-(3-cyclopentyloxy-2-hydroxy-4-methoxyphenyl)-2-(3,5-dichloropyridin-4-yl)ethanone Chemical compound OC1=C(OC2CCCC2)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl OXLLLXVNJUIDJX-UHFFFAOYSA-N 0.000 claims 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims 2
- VSYDBUNFIWMARN-UHFFFAOYSA-N 1-[2,3-bis(difluoromethoxy)-4-methoxyphenyl]-2-(3,5-dichloropyridin-4-yl)ethanone Chemical compound FC(F)OC1=C(OC(F)F)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl VSYDBUNFIWMARN-UHFFFAOYSA-N 0.000 claims 2
- DTYNTAQEFRZTOF-UHFFFAOYSA-N 1-[2-(2-cyclohexylethoxy)-3,4-dimethoxyphenyl]-2-(3,5-dichloropyridin-4-yl)ethanone Chemical compound C1CCCCC1CCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl DTYNTAQEFRZTOF-UHFFFAOYSA-N 0.000 claims 2
- VWZKDNCXKKHULU-UHFFFAOYSA-N 1-[2-[(2-chlorophenyl)methoxy]-3,4-dimethoxyphenyl]-2-(3,5-dichloropyridin-4-yl)ethanone Chemical compound C=1C=CC=C(Cl)C=1COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl VWZKDNCXKKHULU-UHFFFAOYSA-N 0.000 claims 2
- UUALYBMSYGWDOD-UHFFFAOYSA-N 1-[2-[(3-chlorophenyl)methoxy]-3,4-dimethoxyphenyl]-2-(3,5-dichloropyridin-4-yl)ethanone Chemical compound C=1C=CC(Cl)=CC=1COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl UUALYBMSYGWDOD-UHFFFAOYSA-N 0.000 claims 2
- FAUONCLSIFGBAE-UHFFFAOYSA-N 1-[2-[(4-chlorophenyl)methoxy]-3,4-dimethoxyphenyl]-2-(3,5-dichloropyridin-4-yl)ethanone Chemical compound C=1C=C(Cl)C=CC=1COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl FAUONCLSIFGBAE-UHFFFAOYSA-N 0.000 claims 2
- AUDYFIBIJYSVQY-UHFFFAOYSA-N 1-[2-[(5-chlorothiophen-2-yl)methoxy]-3,4-dimethoxyphenyl]-2-(3,5-dichloropyridin-4-yl)ethanone Chemical compound C=1C=C(Cl)SC=1COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl AUDYFIBIJYSVQY-UHFFFAOYSA-N 0.000 claims 2
- DOQIRWPNZIGHBL-UHFFFAOYSA-N 1-[2-[2-(3-bromophenyl)ethoxy]-3,4-dimethoxyphenyl]-2-(3,5-dichloropyridin-4-yl)ethanone Chemical compound C=1C=CC(Br)=CC=1CCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl DOQIRWPNZIGHBL-UHFFFAOYSA-N 0.000 claims 2
- MJJGEGJEFXULAU-UHFFFAOYSA-N 1-[2-[2-(4-chlorophenoxy)ethoxy]-3,4-dimethoxyphenyl]-2-(3,5-dichloropyridin-4-yl)ethanone Chemical compound C=1C=C(Cl)C=CC=1OCCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl MJJGEGJEFXULAU-UHFFFAOYSA-N 0.000 claims 2
- FIWOJRHNMZWIII-UHFFFAOYSA-N 1-[2-[2-(4-chlorophenyl)ethoxy]-3,4-dimethoxyphenyl]-2-(3,5-dichloropyridin-4-yl)ethanone Chemical compound C=1C=C(Cl)C=CC=1CCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl FIWOJRHNMZWIII-UHFFFAOYSA-N 0.000 claims 2
- XGNROMYEANDWBV-UHFFFAOYSA-N 1-[3-(cyclopropylmethoxy)-2,4-dimethoxyphenyl]-2-(3,5-dichloropyridin-4-yl)ethanone Chemical compound COC1=C(OCC2CC2)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl XGNROMYEANDWBV-UHFFFAOYSA-N 0.000 claims 2
- OTRTVVFKCITNML-UHFFFAOYSA-N 1-[3-(cyclopropylmethoxy)-2-hydroxy-4-methoxyphenyl]-2-(3,5-dichloropyridin-4-yl)ethanone Chemical compound OC1=C(OCC2CC2)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl OTRTVVFKCITNML-UHFFFAOYSA-N 0.000 claims 2
- SKUOFNDSDASKRV-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-(2,3-diethoxy-4-methoxyphenyl)ethanone Chemical compound CCOC1=C(OC)C=CC(C(=O)CC=2C(=CN=CC=2Cl)Cl)=C1OCC SKUOFNDSDASKRV-UHFFFAOYSA-N 0.000 claims 2
- RLWQQEHPJNNTGF-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-(2,4-dimethoxy-3-pent-2-enoxyphenyl)ethanone Chemical compound CCC=CCOC1=C(OC)C=CC(C(=O)CC=2C(=CN=CC=2Cl)Cl)=C1OC RLWQQEHPJNNTGF-UHFFFAOYSA-N 0.000 claims 2
- ASJWCPHMNSBYKS-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-(2,4-dimethoxy-3-phenylmethoxyphenyl)ethanone Chemical compound COC1=C(OCC=2C=CC=CC=2)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl ASJWCPHMNSBYKS-UHFFFAOYSA-N 0.000 claims 2
- NBXASMDRACSYCU-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-(2,4-dimethoxy-3-prop-2-ynoxyphenyl)ethanone Chemical compound COC1=C(OCC#C)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl NBXASMDRACSYCU-UHFFFAOYSA-N 0.000 claims 2
- UUYBYQPDBPQDRD-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-(2-hexoxy-3,4-dimethoxyphenyl)ethanone Chemical compound C1=CC(OC)=C(OC)C(OCCCCCC)=C1C(=O)CC1=C(Cl)C=NC=C1Cl UUYBYQPDBPQDRD-UHFFFAOYSA-N 0.000 claims 2
- CYKNNTIKSOVHEQ-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-(2-hydroxy-4-methoxy-3-prop-2-enoxyphenyl)ethanone Chemical compound OC1=C(OCC=C)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl CYKNNTIKSOVHEQ-UHFFFAOYSA-N 0.000 claims 2
- CQNYAUULEGLSKX-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-(3,4-dimethoxy-2-pent-2-enoxyphenyl)ethanone Chemical compound CCC=CCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl CQNYAUULEGLSKX-UHFFFAOYSA-N 0.000 claims 2
- MZVCROAJYCFFBU-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-(3,4-dimethoxy-2-pent-4-enoxyphenyl)ethanone Chemical compound C=CCCCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl MZVCROAJYCFFBU-UHFFFAOYSA-N 0.000 claims 2
- ZUZGIAAQIMTXJZ-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-(3,4-dimethoxy-2-phenylmethoxyphenyl)ethanone Chemical compound C=1C=CC=CC=1COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl ZUZGIAAQIMTXJZ-UHFFFAOYSA-N 0.000 claims 2
- OUECCBYYAPBBGU-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-(3-ethoxy-2,4-dimethoxyphenyl)ethanone Chemical compound CCOC1=C(OC)C=CC(C(=O)CC=2C(=CN=CC=2Cl)Cl)=C1OC OUECCBYYAPBBGU-UHFFFAOYSA-N 0.000 claims 2
- SDZOJIYKTNKVMO-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-(3-ethoxy-2-hydroxy-4-methoxyphenyl)ethanone Chemical compound C1=C(OC)C(OCC)=C(O)C(C(=O)CC=2C(=CN=CC=2Cl)Cl)=C1 SDZOJIYKTNKVMO-UHFFFAOYSA-N 0.000 claims 2
- BFSZKUJJMOONNH-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-(3-hydroxy-2,4-dimethoxyphenyl)ethanone Chemical compound COC1=C(O)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl BFSZKUJJMOONNH-UHFFFAOYSA-N 0.000 claims 2
- JJPBTJGCARKTTP-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[2,4-dimethoxy-3-(2-methoxyethoxy)phenyl]ethanone Chemical compound COCCOC1=C(OC)C=CC(C(=O)CC=2C(=CN=CC=2Cl)Cl)=C1OC JJPBTJGCARKTTP-UHFFFAOYSA-N 0.000 claims 2
- ZXQWTZAJNLCAEQ-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[2,4-dimethoxy-3-(2-phenylethoxy)phenyl]ethanone Chemical compound COC1=C(OCCC=2C=CC=CC=2)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl ZXQWTZAJNLCAEQ-UHFFFAOYSA-N 0.000 claims 2
- QGORXUZXGJYAGV-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[2,4-dimethoxy-3-(4-methylpent-3-enoxy)phenyl]ethanone Chemical compound COC1=C(OCCC=C(C)C)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl QGORXUZXGJYAGV-UHFFFAOYSA-N 0.000 claims 2
- DVEVGBSUTXMHHE-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[2-(2-ethylbutoxy)-3,4-dimethoxyphenyl]ethanone Chemical compound C1=CC(OC)=C(OC)C(OCC(CC)CC)=C1C(=O)CC1=C(Cl)C=NC=C1Cl DVEVGBSUTXMHHE-UHFFFAOYSA-N 0.000 claims 2
- VPTJUCWNNSOTPJ-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[2-(2-hydroxyethoxy)-3,4-dimethoxyphenyl]ethanone Chemical compound OCCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl VPTJUCWNNSOTPJ-UHFFFAOYSA-N 0.000 claims 2
- WUYLGHHVSYUCOT-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[2-[(2,3-difluoro-4-methylphenyl)methoxy]-3,4-dimethoxyphenyl]ethanone Chemical compound C=1C=C(C)C(F)=C(F)C=1COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl WUYLGHHVSYUCOT-UHFFFAOYSA-N 0.000 claims 2
- UUPHXBRXXQYUGE-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[2-[(2-fluorophenyl)methoxy]-3,4-dimethoxyphenyl]ethanone Chemical compound C=1C=CC=C(F)C=1COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl UUPHXBRXXQYUGE-UHFFFAOYSA-N 0.000 claims 2
- LIADZBYPVJGPAC-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[2-[(4-fluorophenyl)methoxy]-3,4-dimethoxyphenyl]ethanone Chemical compound C=1C=C(F)C=CC=1COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl LIADZBYPVJGPAC-UHFFFAOYSA-N 0.000 claims 2
- BOVSNWBYIPDQLD-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[2-[2-(4-fluorophenyl)ethoxy]-3,4-dimethoxyphenyl]ethanone Chemical compound C=1C=C(F)C=CC=1CCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl BOVSNWBYIPDQLD-UHFFFAOYSA-N 0.000 claims 2
- UDJXJYWFLLZCTC-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[2-[[2-(difluoromethoxy)phenyl]methoxy]-3,4-dimethoxyphenyl]ethanone Chemical compound C=1C=CC=C(OC(F)F)C=1COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl UDJXJYWFLLZCTC-UHFFFAOYSA-N 0.000 claims 2
- VHLHWBCYWSRXDA-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[2-[[2-fluoro-6-(trifluoromethyl)phenyl]methoxy]-3,4-dimethoxyphenyl]ethanone Chemical compound FC=1C=CC=C(C(F)(F)F)C=1COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl VHLHWBCYWSRXDA-UHFFFAOYSA-N 0.000 claims 2
- YMGQRHRYJZAXSJ-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[2-[[3-fluoro-5-(trifluoromethyl)phenyl]methoxy]-3,4-dimethoxyphenyl]ethanone Chemical compound C=1C(F)=CC(C(F)(F)F)=CC=1COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl YMGQRHRYJZAXSJ-UHFFFAOYSA-N 0.000 claims 2
- DTNGOQXPWQAEBQ-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-(1-phenylpropan-2-yloxy)phenyl]ethanone Chemical compound C=1C=CC=CC=1CC(C)OC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl DTNGOQXPWQAEBQ-UHFFFAOYSA-N 0.000 claims 2
- YAWQDHGBQCPQID-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-(1-phenylpropoxy)phenyl]ethanone Chemical compound C=1C=CC=CC=1C(CC)OC(C(=C(OC)C=C1)OC)=C1C(=O)CC1=C(Cl)C=NC=C1Cl YAWQDHGBQCPQID-UHFFFAOYSA-N 0.000 claims 2
- QGZHZKISGDRSGJ-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-(2-methoxyethoxy)phenyl]ethanone Chemical compound C1=CC(OC)=C(OC)C(OCCOC)=C1C(=O)CC1=C(Cl)C=NC=C1Cl QGZHZKISGDRSGJ-UHFFFAOYSA-N 0.000 claims 2
- VTZDKIZZAJHJRK-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-(2-methylpropoxy)phenyl]ethanone Chemical compound CC(C)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl VTZDKIZZAJHJRK-UHFFFAOYSA-N 0.000 claims 2
- XVPBIMZNBYDQEM-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-(2-phenylpropoxy)phenyl]ethanone Chemical compound C=1C=CC=CC=1C(C)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl XVPBIMZNBYDQEM-UHFFFAOYSA-N 0.000 claims 2
- NOKIKIMOIGWLOD-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-(2-pyridin-3-ylethoxy)phenyl]ethanone Chemical compound C=1C=CN=CC=1CCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl NOKIKIMOIGWLOD-UHFFFAOYSA-N 0.000 claims 2
- DPXLJUYLWIVAPU-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-(2-pyridin-4-ylethoxy)phenyl]ethanone Chemical compound C=1C=NC=CC=1CCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl DPXLJUYLWIVAPU-UHFFFAOYSA-N 0.000 claims 2
- ZUEQMUBWLSDUJJ-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-(3-methylbut-2-enoxy)phenyl]ethanone Chemical compound CC(C)=CCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl ZUEQMUBWLSDUJJ-UHFFFAOYSA-N 0.000 claims 2
- TZJWDASQNDQUNO-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-(3-methylbutoxy)phenyl]ethanone Chemical compound CC(C)CCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl TZJWDASQNDQUNO-UHFFFAOYSA-N 0.000 claims 2
- BUMMGBAYAPXUBP-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-(3-phenoxypropoxy)phenyl]ethanone Chemical compound C=1C=CC=CC=1OCCCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl BUMMGBAYAPXUBP-UHFFFAOYSA-N 0.000 claims 2
- KOHXGYZDGINMGH-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-(3-phenylpropoxy)phenyl]ethanone Chemical compound C=1C=CC=CC=1CCCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl KOHXGYZDGINMGH-UHFFFAOYSA-N 0.000 claims 2
- VCZXNLUGQYGLGR-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-(5-methylhexoxy)phenyl]ethanone Chemical compound CC(C)CCCCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl VCZXNLUGQYGLGR-UHFFFAOYSA-N 0.000 claims 2
- IOBPYOLVXMNYCA-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-(naphthalen-2-ylmethoxy)phenyl]ethanone Chemical compound C=1C=C2C=CC=CC2=CC=1COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl IOBPYOLVXMNYCA-UHFFFAOYSA-N 0.000 claims 2
- CJOMHHRTMYLZAU-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-[(2-methylquinolin-6-yl)methoxy]phenyl]ethanone Chemical compound C=1C=C2N=C(C)C=CC2=CC=1COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl CJOMHHRTMYLZAU-UHFFFAOYSA-N 0.000 claims 2
- FKVZZYPDIZUKTJ-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-[(3-methoxyphenyl)methoxy]phenyl]ethanone Chemical compound COC1=CC=CC(COC=2C(=C(OC)C=CC=2C(=O)CC=2C(=CN=CC=2Cl)Cl)OC)=C1 FKVZZYPDIZUKTJ-UHFFFAOYSA-N 0.000 claims 2
- VRMIIPPAVGSUCU-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-[(3-methylphenyl)methoxy]phenyl]ethanone Chemical compound C=1C=CC(C)=CC=1COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl VRMIIPPAVGSUCU-UHFFFAOYSA-N 0.000 claims 2
- RQKKDOIXCSBOBP-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-[(4-methoxyphenyl)methoxy]phenyl]ethanone Chemical compound C1=CC(OC)=CC=C1COC1=C(C(=O)CC=2C(=CN=CC=2Cl)Cl)C=CC(OC)=C1OC RQKKDOIXCSBOBP-UHFFFAOYSA-N 0.000 claims 2
- MODAQTRGUVRBRE-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-[(4-propan-2-ylphenyl)methoxy]phenyl]ethanone Chemical compound C=1C=C(C(C)C)C=CC=1COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl MODAQTRGUVRBRE-UHFFFAOYSA-N 0.000 claims 2
- MDMXGGDDKAESJV-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-[(5-methyl-1,2-oxazol-3-yl)methoxy]phenyl]ethanone Chemical compound C1=C(C)ON=C1COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl MDMXGGDDKAESJV-UHFFFAOYSA-N 0.000 claims 2
- CNEKTFIPGQMVJW-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-[2-(3-methoxyphenyl)ethoxy]phenyl]ethanone Chemical compound COC1=CC=CC(CCOC=2C(=C(OC)C=CC=2C(=O)CC=2C(=CN=CC=2Cl)Cl)OC)=C1 CNEKTFIPGQMVJW-UHFFFAOYSA-N 0.000 claims 2
- DQTZKBDPTUNLNM-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-[2-(4-methoxyphenyl)ethoxy]phenyl]ethanone Chemical compound C1=CC(OC)=CC=C1CCOC1=C(C(=O)CC=2C(=CN=CC=2Cl)Cl)C=CC(OC)=C1OC DQTZKBDPTUNLNM-UHFFFAOYSA-N 0.000 claims 2
- WRQVXZJNJVCBAV-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-[2-(4-methylphenyl)-2-oxoethoxy]phenyl]ethanone Chemical compound C=1C=C(C)C=CC=1C(=O)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl WRQVXZJNJVCBAV-UHFFFAOYSA-N 0.000 claims 2
- HZZHHQWQKFBILS-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-[2-(4-methylphenyl)ethoxy]phenyl]ethanone Chemical compound C=1C=C(C)C=CC=1CCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl HZZHHQWQKFBILS-UHFFFAOYSA-N 0.000 claims 2
- MVCJYUVOROQFLV-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-[2-(4-methylsulfonylphenyl)ethoxy]phenyl]ethanone Chemical compound C=1C=C(S(C)(=O)=O)C=CC=1CCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl MVCJYUVOROQFLV-UHFFFAOYSA-N 0.000 claims 2
- FZCNCMRCAWZIOE-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-[[3-(trifluoromethoxy)phenyl]methoxy]phenyl]ethanone Chemical compound C=1C=CC(OC(F)(F)F)=CC=1COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl FZCNCMRCAWZIOE-UHFFFAOYSA-N 0.000 claims 2
- FZZIYKNFYHUBKK-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3,4-dimethoxy-2-[[3-(trifluoromethyl)phenyl]methoxy]phenyl]ethanone Chemical compound C=1C=CC(C(F)(F)F)=CC=1COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl FZZIYKNFYHUBKK-UHFFFAOYSA-N 0.000 claims 2
- PSNIDYIRGAGYGG-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3-(2-hydroxyethoxy)-2,4-dimethoxyphenyl]ethanone Chemical compound COC1=C(OCCO)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl PSNIDYIRGAGYGG-UHFFFAOYSA-N 0.000 claims 2
- FOMTWKFXAKGMPS-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[3-ethoxy-4-methoxy-2-(2-phenylethoxy)phenyl]ethanone Chemical compound C=1C=CC=CC=1CCOC=1C(OCC)=C(OC)C=CC=1C(=O)CC1=C(Cl)C=NC=C1Cl FOMTWKFXAKGMPS-UHFFFAOYSA-N 0.000 claims 2
- PDOHITFVBCRDID-UHFFFAOYSA-N 2-(3,5-dichloropyridin-4-yl)-1-[4-ethoxy-3-methoxy-2-(2-phenylethoxy)phenyl]ethanone Chemical compound C=1C=CC=CC=1CCOC1=C(OC)C(OCC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl PDOHITFVBCRDID-UHFFFAOYSA-N 0.000 claims 2
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- GTELPGRUGWWEFG-UHFFFAOYSA-N 2-[2,3-dimethoxy-6-(2-pyrazin-2-ylacetyl)phenoxy]-n-propylacetamide Chemical compound C1=CC(OC)=C(OC)C(OCC(=O)NCCC)=C1C(=O)CC1=CN=CC=N1 GTELPGRUGWWEFG-UHFFFAOYSA-N 0.000 claims 2
- PPOVHFHWVQELQL-UHFFFAOYSA-N 2-[2,3-dimethoxy-6-(2-pyridazin-3-ylacetyl)phenoxy]-n-propylacetamide Chemical compound C1=CC(OC)=C(OC)C(OCC(=O)NCCC)=C1C(=O)CC1=CC=CN=N1 PPOVHFHWVQELQL-UHFFFAOYSA-N 0.000 claims 2
- SAHVXWZBQAFGSI-UHFFFAOYSA-N 2-[2,3-dimethoxy-6-(2-pyridin-4-ylacetyl)phenoxy]-n-propylacetamide Chemical compound C1=CC(OC)=C(OC)C(OCC(=O)NCCC)=C1C(=O)CC1=CC=NC=C1 SAHVXWZBQAFGSI-UHFFFAOYSA-N 0.000 claims 2
- GOVSWHMHBSRKRD-UHFFFAOYSA-N 2-[2,3-dimethoxy-6-(2-quinolin-4-ylacetyl)phenoxy]-n-propylacetamide Chemical compound C1=CC(OC)=C(OC)C(OCC(=O)NCCC)=C1C(=O)CC1=CC=NC2=CC=CC=C12 GOVSWHMHBSRKRD-UHFFFAOYSA-N 0.000 claims 2
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- MXWZBLXSYIHAKD-UHFFFAOYSA-N 2-[2-(tert-butylamino)-3,5-dichloropyridin-4-yl]-1-[2-[2-(4-fluorophenyl)ethoxy]-3,4-dimethoxyphenyl]ethanone Chemical compound C=1C=C(F)C=CC=1CCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC(NC(C)(C)C)=C1Cl MXWZBLXSYIHAKD-UHFFFAOYSA-N 0.000 claims 2
- ZJLHGVYDTFGFSU-UHFFFAOYSA-N 2-[2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]ethyl]isoindole-1,3-dione Chemical compound O=C1C2=CC=CC=C2C(=O)N1CCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl ZJLHGVYDTFGFSU-UHFFFAOYSA-N 0.000 claims 2
- TWMITTAXSZKQCQ-UHFFFAOYSA-N 2-[3-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]propyl]isoindole-1,3-dione Chemical compound O=C1C2=CC=CC=C2C(=O)N1CCCOC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl TWMITTAXSZKQCQ-UHFFFAOYSA-N 0.000 claims 2
- ZHYPFUMETNJBAS-UHFFFAOYSA-N 2-[6-[2-(2,6-dichlorophenyl)acetyl]-2,3-dimethoxyphenoxy]-n-propylacetamide Chemical compound CCCNC(=O)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=CC=C1Cl ZHYPFUMETNJBAS-UHFFFAOYSA-N 0.000 claims 2
- SRDGRNRVWSQIPY-UHFFFAOYSA-N 2-[6-[2-(2-chloropyridin-3-yl)acetyl]-2,3-dimethoxyphenoxy]-n-propylacetamide Chemical compound C1=CC(OC)=C(OC)C(OCC(=O)NCCC)=C1C(=O)CC1=CC=CN=C1Cl SRDGRNRVWSQIPY-UHFFFAOYSA-N 0.000 claims 2
- IUYGCCZNVGAMTQ-UHFFFAOYSA-N 2-[6-[2-(2-cyanopyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-propylacetamide Chemical compound CCCNC(=O)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=CC=NC(C#N)=C1 IUYGCCZNVGAMTQ-UHFFFAOYSA-N 0.000 claims 2
- FZPSRUQKZQAUHY-UHFFFAOYSA-N 2-[6-[2-(3,5-dibromopyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-propylacetamide Chemical compound C1=CC(OC)=C(OC)C(OCC(=O)NCCC)=C1C(=O)CC1=C(Br)C=NC=C1Br FZPSRUQKZQAUHY-UHFFFAOYSA-N 0.000 claims 2
- QLROCGFGPAAMFW-UHFFFAOYSA-N 2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-(2-hydroxyethyl)acetamide Chemical compound OCCNC(=O)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl QLROCGFGPAAMFW-UHFFFAOYSA-N 0.000 claims 2
- DKXYEGNIOKXIKZ-UHFFFAOYSA-N 2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-(2-phenoxyethyl)acetamide Chemical compound C=1C=CC=CC=1OCCNC(=O)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl DKXYEGNIOKXIKZ-UHFFFAOYSA-N 0.000 claims 2
- OHEMRPAPVBTGHV-UHFFFAOYSA-N 2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-(2-phenylethyl)acetamide Chemical compound C=1C=CC=CC=1CCNC(=O)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl OHEMRPAPVBTGHV-UHFFFAOYSA-N 0.000 claims 2
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- XKKGUHTYRDBTBF-UHFFFAOYSA-N 2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-(3-methylbutyl)acetamide Chemical compound CC(C)CCNC(=O)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl XKKGUHTYRDBTBF-UHFFFAOYSA-N 0.000 claims 2
- LMURGDBDJMITHN-UHFFFAOYSA-N 2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-(3-phenylpropyl)acetamide Chemical compound C=1C=CC=CC=1CCCNC(=O)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl LMURGDBDJMITHN-UHFFFAOYSA-N 0.000 claims 2
- OZJYFBGKTLVAOL-UHFFFAOYSA-N 2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-(3-propan-2-yloxypropyl)acetamide Chemical compound CC(C)OCCCNC(=O)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl OZJYFBGKTLVAOL-UHFFFAOYSA-N 0.000 claims 2
- HKNSROOPYNMQTL-UHFFFAOYSA-N 2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-(furan-2-ylmethyl)acetamide Chemical compound C=1C=COC=1CNC(=O)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl HKNSROOPYNMQTL-UHFFFAOYSA-N 0.000 claims 2
- QHPZKVVWEIDCES-UHFFFAOYSA-N 2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-(pyridin-3-ylmethyl)acetamide Chemical compound C=1C=CN=CC=1CNC(=O)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl QHPZKVVWEIDCES-UHFFFAOYSA-N 0.000 claims 2
- GESICGOMVYWZOU-UHFFFAOYSA-N 2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-(pyridin-4-ylmethyl)acetamide Chemical compound C=1C=NC=CC=1CNC(=O)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl GESICGOMVYWZOU-UHFFFAOYSA-N 0.000 claims 2
- DFMCGOTUZIRANW-UHFFFAOYSA-N 2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-[(2-methoxyphenyl)methyl]acetamide Chemical compound COC1=CC=CC=C1CNC(=O)COC1=C(C(=O)CC=2C(=CN=CC=2Cl)Cl)C=CC(OC)=C1OC DFMCGOTUZIRANW-UHFFFAOYSA-N 0.000 claims 2
- JMQFQPXNSUABPG-UHFFFAOYSA-N 2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-[(2-methylphenyl)methyl]acetamide Chemical compound C=1C=CC=C(C)C=1CNC(=O)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl JMQFQPXNSUABPG-UHFFFAOYSA-N 0.000 claims 2
- LFUPPELHGPIHFO-CILPGNKCSA-N 2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-[(2r)-2-hydroxy-2,3-dihydro-1h-inden-1-yl]acetamide Chemical compound C([C@H]1O)C2=CC=CC=C2C1NC(=O)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl LFUPPELHGPIHFO-CILPGNKCSA-N 0.000 claims 2
- MUMWJPRJSGPLNT-NRFANRHFSA-N 2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-[(2r)-2-hydroxy-2-phenylethyl]acetamide Chemical compound C([C@H](O)C=1C=CC=CC=1)NC(=O)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl MUMWJPRJSGPLNT-NRFANRHFSA-N 0.000 claims 2
- MUMWJPRJSGPLNT-OAQYLSRUSA-N 2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-[(2s)-2-hydroxy-2-phenylethyl]acetamide Chemical compound C([C@@H](O)C=1C=CC=CC=1)NC(=O)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl MUMWJPRJSGPLNT-OAQYLSRUSA-N 0.000 claims 2
- JVPFOYGOQMGFDN-UHFFFAOYSA-N 2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-[(3-fluorophenyl)methyl]acetamide Chemical compound C=1C=CC(F)=CC=1CNC(=O)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl JVPFOYGOQMGFDN-UHFFFAOYSA-N 0.000 claims 2
- NTKPBNIVYQNNMP-UHFFFAOYSA-N 2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-[(3-methoxyphenyl)methyl]acetamide Chemical compound COC1=CC=CC(CNC(=O)COC=2C(=C(OC)C=CC=2C(=O)CC=2C(=CN=CC=2Cl)Cl)OC)=C1 NTKPBNIVYQNNMP-UHFFFAOYSA-N 0.000 claims 2
- WYCSOVCXNRWLKJ-UHFFFAOYSA-N 2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-[(3-methylphenyl)methyl]acetamide Chemical compound C=1C=CC(C)=CC=1CNC(=O)COC1=C(OC)C(OC)=CC=C1C(=O)CC1=C(Cl)C=NC=C1Cl WYCSOVCXNRWLKJ-UHFFFAOYSA-N 0.000 claims 2
- YTPBNBBKIGKMLN-UHFFFAOYSA-N 2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-[(4-ethylphenyl)methyl]acetamide Chemical compound C1=CC(CC)=CC=C1CNC(=O)COC1=C(C(=O)CC=2C(=CN=CC=2Cl)Cl)C=CC(OC)=C1OC YTPBNBBKIGKMLN-UHFFFAOYSA-N 0.000 claims 2
- OLDIYUJTPRQJRO-UHFFFAOYSA-N 2-[6-[2-(3,5-dichloropyridin-4-yl)acetyl]-2,3-dimethoxyphenoxy]-n-[(4-methoxyphenyl)methyl]acetamide Chemical compound C1=CC(OC)=CC=C1CNC(=O)COC1=C(C(=O)CC=2C(=CN=CC=2Cl)Cl)C=CC(OC)=C1OC OLDIYUJTPRQJRO-UHFFFAOYSA-N 0.000 claims 2
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- JTSGEWHPQPAXOR-UHFFFAOYSA-N n-cyclopentylacetamide Chemical compound CC(=O)NC1CCCC1 JTSGEWHPQPAXOR-UHFFFAOYSA-N 0.000 claims 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims 1
- LMTGCJANOQOGPI-UHFFFAOYSA-N n-methyl-n-phenylacetamide Chemical compound CC(=O)N(C)C1=CC=CC=C1 LMTGCJANOQOGPI-UHFFFAOYSA-N 0.000 claims 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- PDUSWJORWQPNRP-UHFFFAOYSA-N n-propan-2-ylacetamide Chemical compound CC(C)NC(C)=O PDUSWJORWQPNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- 125000001715 oxadiazolyl group Chemical group 0.000 claims 1
- QMMOXUPEWRXHJS-UHFFFAOYSA-N pent-2-ene Chemical compound CCC=CC QMMOXUPEWRXHJS-UHFFFAOYSA-N 0.000 claims 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 claims 1
- DLRJIFUOBPOJNS-UHFFFAOYSA-N phenetole Chemical compound CCOC1=CC=CC=C1 DLRJIFUOBPOJNS-UHFFFAOYSA-N 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 claims 1
- DSNYFFJTZPIKFZ-UHFFFAOYSA-N propoxybenzene Chemical compound CCCOC1=CC=CC=C1 DSNYFFJTZPIKFZ-UHFFFAOYSA-N 0.000 claims 1
- RPTKMZRQBREOMV-UHFFFAOYSA-N propoxymethylbenzene Chemical compound CCCOCC1=CC=CC=C1 RPTKMZRQBREOMV-UHFFFAOYSA-N 0.000 claims 1
- MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical compound CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 claims 1
- 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims 1
- 125000003373 pyrazinyl group Chemical group 0.000 claims 1
- 125000002206 pyridazin-3-yl group Chemical group [H]C1=C([H])C([H])=C(*)N=N1 0.000 claims 1
- 125000002098 pyridazinyl group Chemical group 0.000 claims 1
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims 1
- 125000005493 quinolyl group Chemical group 0.000 claims 1
- KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 claims 1
- 125000000335 thiazolyl group Chemical group 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 0 *C1(*)*=C(CC(c(ccc(O*)c2O*)c2OC=[U])=O)[C@](C2)C2=*1 Chemical compound *C1(*)*=C(CC(c(ccc(O*)c2O*)c2OC=[U])=O)[C@](C2)C2=*1 0.000 description 2
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| CA2785253A1 (en) | 2009-12-22 | 2011-06-30 | Leo Pharma A/S | Calcipotriol monohydrate nanocrystals |
| EP2515866B1 (en) | 2009-12-22 | 2014-02-19 | Leo Pharma A/S | Pharmaceutical composition comprising solvent mixture and a vitamin d derivative or analogue |
| JP5873439B2 (ja) | 2009-12-22 | 2016-03-01 | レオ ファーマ アクティーゼルスカブ | ビタミンd類似体および溶媒と界面活性剤の混合物を含む皮膚組成物 |
| CN102775345A (zh) * | 2011-05-13 | 2012-11-14 | 上海特化医药科技有限公司 | 制备罗氟司特的方法及中间体 |
| EP2925364A1 (en) * | 2012-11-30 | 2015-10-07 | Leo Pharma A/S | A method of inhibiting the expression of il-22 in activated t-cells |
| WO2014096018A1 (en) * | 2012-12-19 | 2014-06-26 | Leo Pharma A/S | Methods for the preparation of substituted acetophenones |
| SI3587400T1 (sl) | 2013-10-22 | 2024-05-31 | Chiesi Farmaceutici S.P.A. | Postopek za pripravo zaviralca pde4 |
| CN106459081B (zh) | 2014-06-23 | 2019-09-10 | 利奥制药有限公司 | 1,3-苯并二氧杂环戊烯杂环化合物的制备方法 |
| WO2017089347A1 (en) | 2015-11-25 | 2017-06-01 | Inserm (Institut National De La Sante Et De La Recherche Medicale) | Methods and pharmaceutical compositions for the treatment of braf inhibitor resistant melanomas |
| MX385592B (es) | 2015-12-18 | 2025-03-18 | Union Therapeutics As | Metodos para preparacion de compuestos heterociclicos de 1,3-benzodioxol. |
| KR101702648B1 (ko) * | 2016-05-10 | 2017-02-03 | 주식회사 엑티브온 | 피부 외용제용 보존제, 이를 포함하는 화장료 조성물 및 약학 조성물 |
| CN118344381A (zh) | 2017-06-20 | 2024-07-16 | 联合疗法公司 | 用于制备1,3-苯并二氧杂环戊烯杂环化合物的方法 |
| EP3838967A1 (en) | 2019-12-16 | 2021-06-23 | Spago Nanomedical AB | Immobilization of phenolic compounds |
| CN117924243B (zh) * | 2024-01-16 | 2025-09-12 | 沈阳药科大学 | 一种喹啉衍生物及其药用组合物和应用 |
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| GB9401460D0 (en) * | 1994-01-26 | 1994-03-23 | Rhone Poulenc Rorer Ltd | Compositions of matter |
| JP4172817B2 (ja) * | 1995-05-19 | 2008-10-29 | 協和醗酵工業株式会社 | 含酸素複素環化合物 |
| US6514996B2 (en) * | 1995-05-19 | 2003-02-04 | Kyowa Hakko Kogyo Co., Ltd. | Derivatives of benzofuran or benzodioxole |
| WO1998022455A1 (en) * | 1996-11-19 | 1998-05-28 | Kyowa Hakko Kogyo Co., Ltd. | Oxygenic heterocyclic compounds |
| HRP20050905A2 (hr) * | 2003-03-17 | 2006-04-30 | Kyowa Hakko Kogyo Co. | Terapeutski i/ili preventivni agensi za kronične kožne bolesti |
| WO2006040645A1 (en) * | 2004-10-11 | 2006-04-20 | Ranbaxy Laboratories Limited | N-(3,5-dichloropyridin-4-yl)-2,4,5-alkoxy and 2,3,4-alkoxy benzamide derivatives as pde-iv (phophodiesterase type-iv) inhibitors for the treatment of inflammatory diseases such as asthma |
| EP1888528A2 (en) * | 2005-06-10 | 2008-02-20 | Memory Pharmaceuticals Corporation | Phosphodiesterase 4 inhibitors |
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2007
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- 2007-12-21 AT AT07846434T patent/ATE503742T1/de active
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2011
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