CN105209468B - 取代的7‑氮杂二环化合物以及它们作为食欲素受体调节剂的用途 - Google Patents
取代的7‑氮杂二环化合物以及它们作为食欲素受体调节剂的用途 Download PDFInfo
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- CN105209468B CN105209468B CN201480027442.3A CN201480027442A CN105209468B CN 105209468 B CN105209468 B CN 105209468B CN 201480027442 A CN201480027442 A CN 201480027442A CN 105209468 B CN105209468 B CN 105209468B
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- azabicyclo
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- 0 C*C(*)*C(C)**C(C)C[C@@](C)CC(F)(F)F Chemical compound C*C(*)*C(C)**C(C)C[C@@](C)CC(F)(F)F 0.000 description 16
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- YZGQFTARRCFQCV-UHFFFAOYSA-N CC(c1nc(OCC(CC2CC3)C3N2C(c2ccccc2-c2nc(C)n[o]2)=O)ccc1)(F)F Chemical compound CC(c1nc(OCC(CC2CC3)C3N2C(c2ccccc2-c2nc(C)n[o]2)=O)ccc1)(F)F YZGQFTARRCFQCV-UHFFFAOYSA-N 0.000 description 1
- IYPHDANMLUKQIX-UHFFFAOYSA-N CCOC(c1c2ncccc2ccc1OCC)=O Chemical compound CCOC(c1c2ncccc2ccc1OCC)=O IYPHDANMLUKQIX-UHFFFAOYSA-N 0.000 description 1
- YFLCYYTXHOKLLO-UHFFFAOYSA-N CCOc(c(C(N1C2C(COc3ccccn3)CC1CC2)=O)c1)ncc1[Br]=C Chemical compound CCOc(c(C(N1C2C(COc3ccccn3)CC1CC2)=O)c1)ncc1[Br]=C YFLCYYTXHOKLLO-UHFFFAOYSA-N 0.000 description 1
- MDEZQOBXLBSOHL-UHFFFAOYSA-N CCOc1c(C(N(C(CC2)C3)C2C3Nc(cc2)ncc2Br)=O)nc(C)cc1 Chemical compound CCOc1c(C(N(C(CC2)C3)C2C3Nc(cc2)ncc2Br)=O)nc(C)cc1 MDEZQOBXLBSOHL-UHFFFAOYSA-N 0.000 description 1
- PDIIAZWKWPJDTA-UHFFFAOYSA-N CCOc1c(C(N2C3C(COc4ccc(C(F)(F)F)cn4)CC2CC3)=O)nc(C)cc1 Chemical compound CCOc1c(C(N2C3C(COc4ccc(C(F)(F)F)cn4)CC2CC3)=O)nc(C)cc1 PDIIAZWKWPJDTA-UHFFFAOYSA-N 0.000 description 1
- ZMJYZEVDRZLHHA-UHFFFAOYSA-N CCOc1c(C(NC2(CC3)C4C3C(COc3ccccn3)CC24)=O)c(cccc2)c2cc1 Chemical compound CCOc1c(C(NC2(CC3)C4C3C(COc3ccccn3)CC24)=O)c(cccc2)c2cc1 ZMJYZEVDRZLHHA-UHFFFAOYSA-N 0.000 description 1
- JPQNXJPIJRRFQX-UHFFFAOYSA-N CCOc1ccc(cccn2)c2c1C(O)=O Chemical compound CCOc1ccc(cccn2)c2c1C(O)=O JPQNXJPIJRRFQX-UHFFFAOYSA-N 0.000 description 1
- FZMWFGXVRUFCCE-UHFFFAOYSA-N CCOc1nccc(C)c1C(N1C2C(COc3ccccn3)CC1CC2)=O Chemical compound CCOc1nccc(C)c1C(N1C2C(COc3ccccn3)CC1CC2)=O FZMWFGXVRUFCCE-UHFFFAOYSA-N 0.000 description 1
- JQUDDRIJUAMRQP-UHFFFAOYSA-N CN(C(CC1CC2)C2N1C(c1cccc(F)c1-c1ncccn1)=O)c1ccc(C(F)(F)F)cn1 Chemical compound CN(C(CC1CC2)C2N1C(c1cccc(F)c1-c1ncccn1)=O)c1ccc(C(F)(F)F)cn1 JQUDDRIJUAMRQP-UHFFFAOYSA-N 0.000 description 1
- NDWFXPIZCQZFRX-UHFFFAOYSA-N COC(C=CC1C(N(C(CC2)C3)C2C3Nc2ccc(C(F)(F)F)cn2)=O)=CC1[n]1nccn1 Chemical compound COC(C=CC1C(N(C(CC2)C3)C2C3Nc2ccc(C(F)(F)F)cn2)=O)=CC1[n]1nccn1 NDWFXPIZCQZFRX-UHFFFAOYSA-N 0.000 description 1
- XADDVPRBUREVHD-UHFFFAOYSA-N COc(c(C(N(C(CC1)C2)C1C2Nc(cc1)ncc1[Br]=C)=O)ccc1)c1F Chemical compound COc(c(C(N(C(CC1)C2)C1C2Nc(cc1)ncc1[Br]=C)=O)ccc1)c1F XADDVPRBUREVHD-UHFFFAOYSA-N 0.000 description 1
- GAQMSECBJOFMLH-UHFFFAOYSA-N COc1c(C(N2C3C(COc4ccccn4)CC2CC3)=O)c(nccc2)c2cc1 Chemical compound COc1c(C(N2C3C(COc4ccccn4)CC2CC3)=O)c(nccc2)c2cc1 GAQMSECBJOFMLH-UHFFFAOYSA-N 0.000 description 1
- DYZDIWNRWSNVPT-UHFFFAOYSA-N COc1c(C(O)=O)c(N)ccc1 Chemical compound COc1c(C(O)=O)c(N)ccc1 DYZDIWNRWSNVPT-UHFFFAOYSA-N 0.000 description 1
- YXDHBRKFWUOAPG-UHFFFAOYSA-N COc1c(C(O)=O)c(nccc2)c2cc1 Chemical compound COc1c(C(O)=O)c(nccc2)c2cc1 YXDHBRKFWUOAPG-UHFFFAOYSA-N 0.000 description 1
- WKSFERSMQSQZQP-UHFFFAOYSA-N Cc(cc1)cc(C(N2C3C(COc(nc4)ccc4F)CC2CC3)=O)c1-c1ncccn1 Chemical compound Cc(cc1)cc(C(N2C3C(COc(nc4)ccc4F)CC2CC3)=O)c1-c1ncccn1 WKSFERSMQSQZQP-UHFFFAOYSA-N 0.000 description 1
- HQODAXUOPBHZOT-UHFFFAOYSA-N Cc(cc1)cc(C(N2C3C(COc4nc(C)ccc4)CC2CC3)=O)c1-[n]1nccn1 Chemical compound Cc(cc1)cc(C(N2C3C(COc4nc(C)ccc4)CC2CC3)=O)c1-[n]1nccn1 HQODAXUOPBHZOT-UHFFFAOYSA-N 0.000 description 1
- BOIVPFOYSUFNKD-UHFFFAOYSA-N Cc(cc1)nc(C(N(C(CC2)C3)C2C3Nc2nc3ccccc3nc2)=O)c1-c1ncccn1 Chemical compound Cc(cc1)nc(C(N(C(CC2)C3)C2C3Nc2nc3ccccc3nc2)=O)c1-c1ncccn1 BOIVPFOYSUFNKD-UHFFFAOYSA-N 0.000 description 1
- CSTPGELOUGJKMU-UHFFFAOYSA-N Cc(cc1)nc(C(N2C3C(COc(nc4)ncc4F)CC2CC3)=O)c1N1CCCC1 Chemical compound Cc(cc1)nc(C(N2C3C(COc(nc4)ncc4F)CC2CC3)=O)c1N1CCCC1 CSTPGELOUGJKMU-UHFFFAOYSA-N 0.000 description 1
- LUDLPIYVVSTMPA-UHFFFAOYSA-N Cc(cccc1C(N(C(CC2)C34)C2C3N4c2ccc(C(F)(F)F)cn2)=O)c1-c1ncccc1 Chemical compound Cc(cccc1C(N(C(CC2)C34)C2C3N4c2ccc(C(F)(F)F)cn2)=O)c1-c1ncccc1 LUDLPIYVVSTMPA-UHFFFAOYSA-N 0.000 description 1
- RAMZILZCUQMJMP-UHFFFAOYSA-N Cc1cc(C)nc(OCC(CC2CC3)C3N2C(c2cccc(F)c2N2N=CCN2C)=O)n1 Chemical compound Cc1cc(C)nc(OCC(CC2CC3)C3N2C(c2cccc(F)c2N2N=CCN2C)=O)n1 RAMZILZCUQMJMP-UHFFFAOYSA-N 0.000 description 1
- CJOIQEWZMFDNFP-UHFFFAOYSA-N Cc1ccc(C(N2C3C(COc4ncccc4)CC2CC3)=O)c(-[n]2nncc2)n1 Chemical compound Cc1ccc(C(N2C3C(COc4ncccc4)CC2CC3)=O)c(-[n]2nncc2)n1 CJOIQEWZMFDNFP-UHFFFAOYSA-N 0.000 description 1
- UKTPOKIHZUTCCR-PCYAJDSTSA-N Cc1ncc(NC(CC2CC3)C3N2C(c2c(C/N=C\C=C/NC)c([F-])ccc2)=O)nc1 Chemical compound Cc1ncc(NC(CC2CC3)C3N2C(c2c(C/N=C\C=C/NC)c([F-])ccc2)=O)nc1 UKTPOKIHZUTCCR-PCYAJDSTSA-N 0.000 description 1
- ZEYUQFMOPXXFFL-UHFFFAOYSA-N O=C(c(c(-[n]1nccn1)ccc1)c1F)N(C(CC1)CC23)C1C2[O]3c1ccc(C(F)(F)F)cn1 Chemical compound O=C(c(c(-[n]1nccn1)ccc1)c1F)N(C(CC1)CC23)C1C2[O]3c1ccc(C(F)(F)F)cn1 ZEYUQFMOPXXFFL-UHFFFAOYSA-N 0.000 description 1
- NUFXKJOWPLPSAQ-UHFFFAOYSA-N O=C(c(cc(cc1)F)c1-c1ncccn1)N1C2C(COc3ccccn3)CC1CC2 Chemical compound O=C(c(cc(cc1)F)c1-c1ncccn1)N1C2C(COc3ccccn3)CC1CC2 NUFXKJOWPLPSAQ-UHFFFAOYSA-N 0.000 description 1
- BZGUNGQUOUHFND-JWOMPCOYSA-N O=C(c1ccc([C@@H]2F)c2c1N1N=CC=NC1)N1C2CC(CCCOc3nccc(C(F)(F)F)n3)C3C1C3CC2 Chemical compound O=C(c1ccc([C@@H]2F)c2c1N1N=CC=NC1)N1C2CC(CCCOc3nccc(C(F)(F)F)n3)C3C1C3CC2 BZGUNGQUOUHFND-JWOMPCOYSA-N 0.000 description 1
- AIFFVUBPSLZDLR-UHFFFAOYSA-N O=C(c1cccc(F)c1-c1ncc[o]1)N(C(CC1)C2)C1C2Nc(ncc(C(F)(F)F)c1)c1F Chemical compound O=C(c1cccc(F)c1-c1ncc[o]1)N(C(CC1)C2)C1C2Nc(ncc(C(F)(F)F)c1)c1F AIFFVUBPSLZDLR-UHFFFAOYSA-N 0.000 description 1
- RHTRJHAOUGVNFK-UHFFFAOYSA-N O=C(c1cccc2c1nccc2)N1C2C(COc(nc3)ccc3F)CC1CC2 Chemical compound O=C(c1cccc2c1nccc2)N1C2C(COc(nc3)ccc3F)CC1CC2 RHTRJHAOUGVNFK-UHFFFAOYSA-N 0.000 description 1
- CMWBGWUTIHTIEV-UHFFFAOYSA-N O=C(c1ccccc1-c1ncccn1)N(C(CC1)C23)C1C2N3c1ccc(C(F)(F)F)cn1 Chemical compound O=C(c1ccccc1-c1ncccn1)N(C(CC1)C23)C1C2N3c1ccc(C(F)(F)F)cn1 CMWBGWUTIHTIEV-UHFFFAOYSA-N 0.000 description 1
- JEZFHSYPJLVJOS-UHFFFAOYSA-N O=Cc(cc(cc1)F)c1C1=NCCC=N1 Chemical compound O=Cc(cc(cc1)F)c1C1=NCCC=N1 JEZFHSYPJLVJOS-UHFFFAOYSA-N 0.000 description 1
- RQCGQULJYVNAQX-UHFFFAOYSA-N OC(c1c2ncccc2ccc1O)=O Chemical compound OC(c1c2ncccc2ccc1O)=O RQCGQULJYVNAQX-UHFFFAOYSA-N 0.000 description 1
- HTRLPLIHRMYQCG-UHFFFAOYSA-N OCc(cc1)cc(C(N2C3C(COc(nc4)ccc4F)CC2CC3)=O)c1-[n]1nccn1 Chemical compound OCc(cc1)cc(C(N2C3C(COc(nc4)ccc4F)CC2CC3)=O)c1-[n]1nccn1 HTRLPLIHRMYQCG-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/08—Bridged systems
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
- A61K31/423—Oxazoles condensed with carbocyclic rings
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
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- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
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| SG10201900536TA (en) | 2014-03-06 | 2019-02-27 | Shanghai Haiyan Pharmaceutical Tech Co Ltd | Piperidine derivatives as orexin receptor antagonist |
| MX384432B (es) | 2014-06-27 | 2025-03-14 | Asc Eng Solutions Llc | Abrazadera ajustable y cubo para soporte de manguera flexible. |
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| JP6736661B2 (ja) * | 2015-09-04 | 2020-08-05 | ヤンセン ファーマシューティカ エヌ.ベー. | 治療化合物及び合成 |
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| PT3619199T (pt) * | 2017-05-03 | 2021-10-01 | Idorsia Pharmaceuticals Ltd | Preparação de derivados de ácido 2-([1,2,3]triazol-2-il)- benzoico |
| UA125597C2 (uk) * | 2017-08-03 | 2022-04-27 | Такеда Фармасьютікал Компані Лімітед | Гетероциклічна сполука та її застосування |
| CN107573294A (zh) * | 2017-09-19 | 2018-01-12 | 四川大学 | 5‑甲基‑2‑(2h‑1,2,3‑三唑‑2‑基)苯甲酸的合成方法 |
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| US12187737B2 (en) | 2019-06-04 | 2025-01-07 | Hager Biosciences, Llc | Imidazolo derivatives, compositions and methods as orexin antagonists |
| WO2021208976A1 (zh) * | 2020-04-17 | 2021-10-21 | 上海海雁医药科技有限公司 | 固体药物制剂及其制备方法和用途 |
| TWI888599B (zh) * | 2020-07-17 | 2025-07-01 | 日商衛材R&D企管股份有限公司 | 取代哌啶化合物及其用途 |
| JP7591592B2 (ja) * | 2022-01-14 | 2024-11-28 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 置換ピペリジン化合物を含有する医薬 |
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- 2015-09-11 CL CL2015002616A patent/CL2015002616A1/es unknown
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2016
- 2016-09-12 US US15/262,882 patent/US9695183B2/en active Active
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2018
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Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008150364A1 (en) * | 2007-05-23 | 2008-12-11 | Merck & Co., Inc. | Cyclopropyl pyrrolidine orexin receptor antagonists |
| WO2009104155A1 (en) * | 2008-02-21 | 2009-08-27 | Actelion Pharmaceuticals Ltd | 2-aza-bicyclo[2.2.1]heptane derivatives |
| CN101965343A (zh) * | 2008-02-21 | 2011-02-02 | 埃科特莱茵药品有限公司 | 2-氮杂-双环[2.2.1]庚烷衍生物 |
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