CN108864093A - 取代的2-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2-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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- CN108864093A CN108864093A CN201810842686.7A CN201810842686A CN108864093A CN 108864093 A CN108864093 A CN 108864093A CN 201810842686 A CN201810842686 A CN 201810842686A CN 108864093 A CN108864093 A CN 108864093A
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- halogen
- azabicyclo
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- 0 C1*C(C2CC=CCC2)NC1 Chemical compound C1*C(C2CC=CCC2)NC1 0.000 description 15
- FAOHBTJYYAUIPV-UHFFFAOYSA-N C=C(c(nccc1)c1-c1ncccc1F)N1C(C(C2)Oc3ncc(C(F)(F)F)cc3)C2(C2)C2C1 Chemical compound C=C(c(nccc1)c1-c1ncccc1F)N1C(C(C2)Oc3ncc(C(F)(F)F)cc3)C2(C2)C2C1 FAOHBTJYYAUIPV-UHFFFAOYSA-N 0.000 description 1
- DREYRGXURZPHNL-UHFFFAOYSA-N CCCCC(CC)C1NNCN1 Chemical compound CCCCC(CC)C1NNCN1 DREYRGXURZPHNL-UHFFFAOYSA-N 0.000 description 1
- UODSZXVZFBKAGJ-UHFFFAOYSA-N CCOc1c(C(N(CC(C2)C3)C3C2Nc2ncc(C(F)(F)F)cc2)=O)c(nccc2)c2cc1 Chemical compound CCOc1c(C(N(CC(C2)C3)C3C2Nc2ncc(C(F)(F)F)cc2)=O)c(nccc2)c2cc1 UODSZXVZFBKAGJ-UHFFFAOYSA-N 0.000 description 1
- FBMQWKIZVCIJHX-MORLXBONSA-N CCc(cn1)cnc1OC(C[C@](C)(C1)C2)C1N2C(c(nc(C)cc1)c1-c1ncccn1)=O Chemical compound CCc(cn1)cnc1OC(C[C@](C)(C1)C2)C1N2C(c(nc(C)cc1)c1-c1ncccn1)=O FBMQWKIZVCIJHX-MORLXBONSA-N 0.000 description 1
- WVZLCGIQGDVCKB-UHFFFAOYSA-N CN(C(CC(C1)C2)C1N2C(c(cc(cc1)F)c1-[n]1nccn1)=O)c1ncc(C(F)(F)F)cc1 Chemical compound CN(C(CC(C1)C2)C1N2C(c(cc(cc1)F)c1-[n]1nccn1)=O)c1ncc(C(F)(F)F)cc1 WVZLCGIQGDVCKB-UHFFFAOYSA-N 0.000 description 1
- DTGKMEOSLSJFKU-UHFFFAOYSA-N CN(C(CC(C1)C2)C1N2C(c(cccc1)c1-[n]1nccn1)=O)c1ncc(C(F)(F)F)cc1 Chemical compound CN(C(CC(C1)C2)C1N2C(c(cccc1)c1-[n]1nccn1)=O)c1ncc(C(F)(F)F)cc1 DTGKMEOSLSJFKU-UHFFFAOYSA-N 0.000 description 1
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- QJTINLHWJMECEF-UHFFFAOYSA-N COc1cccc(-c2ncccn2)c1C(N1C(C(C2)Oc(cc3)ncc3Cl)C2(C2)C2C1)=O Chemical compound COc1cccc(-c2ncccn2)c1C(N1C(C(C2)Oc(cc3)ncc3Cl)C2(C2)C2C1)=O QJTINLHWJMECEF-UHFFFAOYSA-N 0.000 description 1
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- PHKJXGMOIKCOPR-UHFFFAOYSA-N Cc1n[o]c(-c(cc(cc2)F)c2C(O)=O)n1 Chemical compound Cc1n[o]c(-c(cc(cc2)F)c2C(O)=O)n1 PHKJXGMOIKCOPR-UHFFFAOYSA-N 0.000 description 1
- XLENHTJUYYHTKS-UHFFFAOYSA-N Cc1nc(-c2ncccn2)c(C(N2C(C(C3)Oc4ncc(C(F)F)cc4)C3(C3)C3C2)O)cc1 Chemical compound Cc1nc(-c2ncccn2)c(C(N2C(C(C3)Oc4ncc(C(F)F)cc4)C3(C3)C3C2)O)cc1 XLENHTJUYYHTKS-UHFFFAOYSA-N 0.000 description 1
- IGPUBGBQVDTOBH-UHFFFAOYSA-N O=C(c(c(F)ccc1)c1-c1ncccn1)N(CC(C1)C2)C1C2Oc1ncc(C(F)(F)F)cc1 Chemical compound O=C(c(c(F)ccc1)c1-c1ncccn1)N(CC(C1)C2)C1C2Oc1ncc(C(F)(F)F)cc1 IGPUBGBQVDTOBH-UHFFFAOYSA-N 0.000 description 1
- ZSTUNAYXBTVBLX-UHFFFAOYSA-N O=C(c(c(F)ccc1)c1-c1ncccn1)N1C(C(C2)Nc3ncc(C(F)(F)F)cc3Cl)C2(C2)C2C1 Chemical compound O=C(c(c(F)ccc1)c1-c1ncccn1)N1C(C(C2)Nc3ncc(C(F)(F)F)cc3Cl)C2(C2)C2C1 ZSTUNAYXBTVBLX-UHFFFAOYSA-N 0.000 description 1
- UVKSKIQNYNKZFE-UHFFFAOYSA-N O=C(c(c(F)ccc1)c1-c1ncccn1)N1C(C(C2)Nc3ncc(C(F)(F)F)cc3F)C2(C2)C2C1 Chemical compound O=C(c(c(F)ccc1)c1-c1ncccn1)N1C(C(C2)Nc3ncc(C(F)(F)F)cc3F)C2(C2)C2C1 UVKSKIQNYNKZFE-UHFFFAOYSA-N 0.000 description 1
- SMONOAFNYGZSPI-UHFFFAOYSA-N O=C(c(ccc(F)c1)c1-[n]1nccn1)N(CC(C1)C2)C1C2Oc(cc1)ncc1Br Chemical compound O=C(c(ccc(F)c1)c1-[n]1nccn1)N(CC(C1)C2)C1C2Oc(cc1)ncc1Br SMONOAFNYGZSPI-UHFFFAOYSA-N 0.000 description 1
- VZFXPAMERHZHBE-UHFFFAOYSA-N O=C(c(ccc(F)c1)c1-c1ncccn1)N(CC(CC1)C2)C1C2Oc1ncc(C(F)(F)F)cc1 Chemical compound O=C(c(ccc(F)c1)c1-c1ncccn1)N(CC(CC1)C2)C1C2Oc1ncc(C(F)(F)F)cc1 VZFXPAMERHZHBE-UHFFFAOYSA-N 0.000 description 1
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- RFQXMXBLMXGNTK-UHFFFAOYSA-N O=C(c(cccc1F)c1-c(nc1)ncc1F)N(CC(C1)C2)C1C2Oc1ncc(C(F)(F)F)cc1 Chemical compound O=C(c(cccc1F)c1-c(nc1)ncc1F)N(CC(C1)C2)C1C2Oc1ncc(C(F)(F)F)cc1 RFQXMXBLMXGNTK-UHFFFAOYSA-N 0.000 description 1
- BMVIINOQMUXBCV-UHFFFAOYSA-N O=C(c(cccc1F)c1-c1ncccn1)N(CC(C1)C2)C1C2Oc1nc(C(F)(F)F)ccc1 Chemical compound O=C(c(cccc1F)c1-c1ncccn1)N(CC(C1)C2)C1C2Oc1nc(C(F)(F)F)ccc1 BMVIINOQMUXBCV-UHFFFAOYSA-N 0.000 description 1
- NYFDLRLMIFHOET-UHFFFAOYSA-N O=C(c(cccc1F)c1-c1ncccn1)N(CC(C1)C2)C1C2Oc1nc(nccc2)c2cc1 Chemical compound O=C(c(cccc1F)c1-c1ncccn1)N(CC(C1)C2)C1C2Oc1nc(nccc2)c2cc1 NYFDLRLMIFHOET-UHFFFAOYSA-N 0.000 description 1
- NZAJUGFTUUMQQI-UHFFFAOYSA-N O=C(c1c(-c2ncccc2F)nccc1)N(CC(C1)C2)C2C1Nc1ncc(C(F)(F)F)nc1 Chemical compound O=C(c1c(-c2ncccc2F)nccc1)N(CC(C1)C2)C2C1Nc1ncc(C(F)(F)F)nc1 NZAJUGFTUUMQQI-UHFFFAOYSA-N 0.000 description 1
- DMOGSWQIKPEGKH-UHFFFAOYSA-N O=C(c1cc(F)ccc1-[n]1nccn1)N(CC(C1)C2)C2C1Nc1ncc(C(F)(F)F)cc1 Chemical compound O=C(c1cc(F)ccc1-[n]1nccn1)N(CC(C1)C2)C2C1Nc1ncc(C(F)(F)F)cc1 DMOGSWQIKPEGKH-UHFFFAOYSA-N 0.000 description 1
- VEJWAVKRPRJLDD-UHFFFAOYSA-N O=C(c1cccc(F)c1-[n]1nccn1)N(CC(C1)C2)C1C2Oc1ncc(C(F)(F)F)cc1 Chemical compound O=C(c1cccc(F)c1-[n]1nccn1)N(CC(C1)C2)C1C2Oc1ncc(C(F)(F)F)cc1 VEJWAVKRPRJLDD-UHFFFAOYSA-N 0.000 description 1
- UCRNCTMKKFBSSC-UHFFFAOYSA-N O=C(c1cccc(F)c1-[n]1nccn1)N(CC(CC1)C2)C1C2Nc1ncc(C(F)(F)F)nc1 Chemical compound O=C(c1cccc(F)c1-[n]1nccn1)N(CC(CC1)C2)C1C2Nc1ncc(C(F)(F)F)nc1 UCRNCTMKKFBSSC-UHFFFAOYSA-N 0.000 description 1
- UDIRKXWCDOXFAB-UHFFFAOYSA-N OC(c(cccc1)c1-c(nc1)ncc1F)N(CC(CC1)C2)C1C2Oc1ncc(C(F)(F)F)nc1 Chemical compound OC(c(cccc1)c1-c(nc1)ncc1F)N(CC(CC1)C2)C1C2Oc1ncc(C(F)(F)F)nc1 UDIRKXWCDOXFAB-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- 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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- 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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
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Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008150364A1 (en) * | 2007-05-23 | 2008-12-11 | Merck & Co., Inc. | Cyclopropyl pyrrolidine orexin receptor antagonists |
| 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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