JP2013519675A - アリールメトキシイソインドリン誘導体、それを含む組成物、及びその使用方法 - Google Patents
アリールメトキシイソインドリン誘導体、それを含む組成物、及びその使用方法 Download PDFInfo
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- JP2013519675A JP2013519675A JP2012552978A JP2012552978A JP2013519675A JP 2013519675 A JP2013519675 A JP 2013519675A JP 2012552978 A JP2012552978 A JP 2012552978A JP 2012552978 A JP2012552978 A JP 2012552978A JP 2013519675 A JP2013519675 A JP 2013519675A
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- 0 CCCC1C(CC#CC**(C)CCCC(*)CC)CCC1 Chemical compound CCCC1C(CC#CC**(C)CCCC(*)CC)CCC1 0.000 description 14
- HICLANHSOCZBJK-UHFFFAOYSA-N CC(C)(C)c1c[n](Cc2ccc(/C=[O]\c3cccc4c3CN(C(CCC(N3)=O)C3=O)C4=O)cc2)cn1 Chemical compound CC(C)(C)c1c[n](Cc2ccc(/C=[O]\c3cccc4c3CN(C(CCC(N3)=O)C3=O)C4=O)cc2)cn1 HICLANHSOCZBJK-UHFFFAOYSA-N 0.000 description 1
- GQGYERVIDUEWGM-UHFFFAOYSA-N CC(C)C(CC1)CCN1S(c1ccc(COc2cccc3c2CN(C(CCC(N2)=O)C2=O)C3=O)cc1)(=O)=O Chemical compound CC(C)C(CC1)CCN1S(c1ccc(COc2cccc3c2CN(C(CCC(N2)=O)C2=O)C3=O)cc1)(=O)=O GQGYERVIDUEWGM-UHFFFAOYSA-N 0.000 description 1
- CYNUEEWICXXGBF-UHFFFAOYSA-N CC(C)NCc1ccc(COc2cccc3c2CN(C(CCC(N2)=O)C2=O)C3=O)cc1 Chemical compound CC(C)NCc1ccc(COc2cccc3c2CN(C(CCC(N2)=O)C2=O)C3=O)cc1 CYNUEEWICXXGBF-UHFFFAOYSA-N 0.000 description 1
- URFVNTXABMXWQR-UHFFFAOYSA-N CC(C1)N(Cc2ccc(COc3cccc4c3CN(C(CCC(N3)=O)C3=O)C4=O)cc2)CCC1c(c(F)c1)ccc1F Chemical compound CC(C1)N(Cc2ccc(COc3cccc4c3CN(C(CCC(N3)=O)C3=O)C4=O)cc2)CCC1c(c(F)c1)ccc1F URFVNTXABMXWQR-UHFFFAOYSA-N 0.000 description 1
- GTVBZNRQKHEQRZ-UHFFFAOYSA-N CC(CC=C1)(C(CN2C(CCC(N3)=O)C3=O)=C1OCc1ccc(CN3CCN(CC(F)(F)F)CC3)cc1)C2=O Chemical compound CC(CC=C1)(C(CN2C(CCC(N3)=O)C3=O)=C1OCc1ccc(CN3CCN(CC(F)(F)F)CC3)cc1)C2=O GTVBZNRQKHEQRZ-UHFFFAOYSA-N 0.000 description 1
- ZEMMFINIEPJEPC-UHFFFAOYSA-N CC1(C(F)(F)F)N(Cc2ccc(COc3cccc4c3CN(C(CCC(N3)=O)C3=O)C4=O)cc2)CCCC1 Chemical compound CC1(C(F)(F)F)N(Cc2ccc(COc3cccc4c3CN(C(CCC(N3)=O)C3=O)C4=O)cc2)CCCC1 ZEMMFINIEPJEPC-UHFFFAOYSA-N 0.000 description 1
- DMTSORWOCIZLHG-UHFFFAOYSA-N CCCC(NC(CN(Cc1c2cccc1OCc(cc1)ccc1S(N(CC1)CCN1c1ccccc1)(=O)=O)C2=O)=O)=O Chemical compound CCCC(NC(CN(Cc1c2cccc1OCc(cc1)ccc1S(N(CC1)CCN1c1ccccc1)(=O)=O)C2=O)=O)=O DMTSORWOCIZLHG-UHFFFAOYSA-N 0.000 description 1
- YTGCBSUEUWLVBM-UHFFFAOYSA-N CCCCN(CCN(Cc1ccc(COc2cccc3c2CN(C(CCC(N2)=O)C2=O)C3=O)cc1)C1)C1=O Chemical compound CCCCN(CCN(Cc1ccc(COc2cccc3c2CN(C(CCC(N2)=O)C2=O)C3=O)cc1)C1)C1=O YTGCBSUEUWLVBM-UHFFFAOYSA-N 0.000 description 1
- KMWNDCPXBMMTLX-UHFFFAOYSA-N CCCOC1CN(Cc2ccc(COc3cccc4c3CN(C(CCC(N3)=O)C3=O)C4=O)cc2)C1 Chemical compound CCCOC1CN(Cc2ccc(COc3cccc4c3CN(C(CCC(N3)=O)C3=O)C4=O)cc2)C1 KMWNDCPXBMMTLX-UHFFFAOYSA-N 0.000 description 1
- LBXNMRHTRGXQSB-UHFFFAOYSA-O CC[S+](N1CCN(Cc2ccc(COc3cccc4c3CN(C(CCC(N3)=O)C3=O)C4=O)cc2)CC1)O Chemical compound CC[S+](N1CCN(Cc2ccc(COc3cccc4c3CN(C(CCC(N3)=O)C3=O)C4=O)cc2)CC1)O LBXNMRHTRGXQSB-UHFFFAOYSA-O 0.000 description 1
- WUICFPKGJHSORB-UHFFFAOYSA-N CCc(c(OCc1ccc(CN(CC2)CCC2N(C)C)cc1)ccc1)c1C(NC(CCC(N1)=O)C1=O)=O Chemical compound CCc(c(OCc1ccc(CN(CC2)CCC2N(C)C)cc1)ccc1)c1C(NC(CCC(N1)=O)C1=O)=O WUICFPKGJHSORB-UHFFFAOYSA-N 0.000 description 1
- POIQCLYZLBEBOB-UHFFFAOYSA-N Cc1cc(C2CCN(Cc3ccc(COc4cccc5c4CCC(CC(CCC(N4)=O)C4=O)C5=O)cc3)CC2)cc(F)c1 Chemical compound Cc1cc(C2CCN(Cc3ccc(COc4cccc5c4CCC(CC(CCC(N4)=O)C4=O)C5=O)cc3)CC2)cc(F)c1 POIQCLYZLBEBOB-UHFFFAOYSA-N 0.000 description 1
- WEJKBJAESOAOMA-UHFFFAOYSA-N NC(C(CCC=O)N(Cc1c2ccc(Cl)c1OCc1ccc(CN3CCOCC3)cc1)C2O)=O Chemical compound NC(C(CCC=O)N(Cc1c2ccc(Cl)c1OCc1ccc(CN3CCOCC3)cc1)C2O)=O WEJKBJAESOAOMA-UHFFFAOYSA-N 0.000 description 1
- LZWYEAULTHQSAP-UHFFFAOYSA-N NCc1ccc(COc2cccc3c2CN(C(CCC(N2)=O)C2=O)C3=O)cc1 Chemical compound NCc1ccc(COc2cccc3c2CN(C(CCC(N2)=O)C2=O)C3=O)cc1 LZWYEAULTHQSAP-UHFFFAOYSA-N 0.000 description 1
- DFRAMWCJSCKHFX-UHFFFAOYSA-N O=C(C(C1C2)=CC=CC1OCc1ccc(CN(CC3)CCN3S(c3ccccc3)(=O)=O)cc1)N2C(CCC(N1)=O)C1=O Chemical compound O=C(C(C1C2)=CC=CC1OCc1ccc(CN(CC3)CCN3S(c3ccccc3)(=O)=O)cc1)N2C(CCC(N1)=O)C1=O DFRAMWCJSCKHFX-UHFFFAOYSA-N 0.000 description 1
- FFBKNPMKKBPKQD-UHFFFAOYSA-N O=C(CCC1N(Cc2ccc3)Cc2c3OCc2ccc(CN(CC3)Cc4c3cccc4)cc2)NC1=O Chemical compound O=C(CCC1N(Cc2ccc3)Cc2c3OCc2ccc(CN(CC3)Cc4c3cccc4)cc2)NC1=O FFBKNPMKKBPKQD-UHFFFAOYSA-N 0.000 description 1
- DPEHVGQOIWFFLT-UHFFFAOYSA-N O=C(c1c(C2)c(/[O]=C\c3ccc(CN4C=CN(CC5CC5)CC4)cc3)ccc1)N2C(CCC(N1)=O)C1=O Chemical compound O=C(c1c(C2)c(/[O]=C\c3ccc(CN4C=CN(CC5CC5)CC4)cc3)ccc1)N2C(CCC(N1)=O)C1=O DPEHVGQOIWFFLT-UHFFFAOYSA-N 0.000 description 1
- YBVZZBQNXYNIOF-UHFFFAOYSA-N O=C(c1c(C2)c(OCc3cc(ccc(CC4CCOCCC4)c4)c4[o]3)ccc1)N2C(CCC(N1)=O)C1=O Chemical compound O=C(c1c(C2)c(OCc3cc(ccc(CC4CCOCCC4)c4)c4[o]3)ccc1)N2C(CCC(N1)=O)C1=O YBVZZBQNXYNIOF-UHFFFAOYSA-N 0.000 description 1
- ONQQXRNSBVAGKT-UHFFFAOYSA-N O=C(c1c(C2)c(OCc3ccc(CN(CC4)CCN4c4ncccn4)cc3)ccc1)N2C(CCC(N1)=O)C1=O Chemical compound O=C(c1c(C2)c(OCc3ccc(CN(CC4)CCN4c4ncccn4)cc3)ccc1)N2C(CCC(N1)=O)C1=O ONQQXRNSBVAGKT-UHFFFAOYSA-N 0.000 description 1
- ZFUAQTOUSWHTBG-UHFFFAOYSA-N O=C(c1c(C2)c(OCc3ccc(CN(CCC4)CC4(F)F)cc3)ccc1)N2C(CCC(N1)=O)C1=O Chemical compound O=C(c1c(C2)c(OCc3ccc(CN(CCC4)CC4(F)F)cc3)ccc1)N2C(CCC(N1)=O)C1=O ZFUAQTOUSWHTBG-UHFFFAOYSA-N 0.000 description 1
- DRDDTMMTRCKSIB-UHFFFAOYSA-N O=C(c1cccc(OCc(cccc2Cl)c2Cl)c1C1)N1C(CCC(N1)=O)C1=O Chemical compound O=C(c1cccc(OCc(cccc2Cl)c2Cl)c1C1)N1C(CCC(N1)=O)C1=O DRDDTMMTRCKSIB-UHFFFAOYSA-N 0.000 description 1
- DQYGFVWJSUFBGN-UHFFFAOYSA-N O=CNCCCCN1CCCCCC1 Chemical compound O=CNCCCCN1CCCCCC1 DQYGFVWJSUFBGN-UHFFFAOYSA-N 0.000 description 1
- YCLYZBAECUNNCS-UHFFFAOYSA-N OC(C(CC1)N(Cc2c3cccc2OCc(cc2)ccc2C(N2CCNCC2)=O)C3=O)NC1=O Chemical compound OC(C(CC1)N(Cc2c3cccc2OCc(cc2)ccc2C(N2CCNCC2)=O)C3=O)NC1=O YCLYZBAECUNNCS-UHFFFAOYSA-N 0.000 description 1
- BFZWNNJXIOPRPI-UHFFFAOYSA-N OCC1C=CC(COc2cccc(C(N3C(CCC(N4)O)C4=O)=O)c2C3=O)=CC1 Chemical compound OCC1C=CC(COc2cccc(C(N3C(CCC(N4)O)C4=O)=O)c2C3=O)=CC1 BFZWNNJXIOPRPI-UHFFFAOYSA-N 0.000 description 1
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- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
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- C07D471/04—Ortho-condensed systems
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- C07D487/04—Ortho-condensed systems
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