KR101908255B1 - 베타세크리타아제 저해제 - Google Patents
베타세크리타아제 저해제 Download PDFInfo
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- KR101908255B1 KR101908255B1 KR1020177032350A KR20177032350A KR101908255B1 KR 101908255 B1 KR101908255 B1 KR 101908255B1 KR 1020177032350 A KR1020177032350 A KR 1020177032350A KR 20177032350 A KR20177032350 A KR 20177032350A KR 101908255 B1 KR101908255 B1 KR 101908255B1
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- South Korea
- Prior art keywords
- alkyl
- alkoxy
- halo
- cycloalkyl
- mmol
- Prior art date
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- 0 **(CCCCC1)CCCC11c2ccccc2*C1(*)* Chemical compound **(CCCCC1)CCCC11c2ccccc2*C1(*)* 0.000 description 22
- RVLIRWFNCYASBC-UHFFFAOYSA-N CN1C(N)=NC2(c3cc(Br)ccc3CC2(CC2)CCC2OC)C1=O Chemical compound CN1C(N)=NC2(c3cc(Br)ccc3CC2(CC2)CCC2OC)C1=O RVLIRWFNCYASBC-UHFFFAOYSA-N 0.000 description 2
- SEQHEDQNODAFIU-UHFFFAOYSA-N O=C1c2cc(Br)ccc2CC1 Chemical compound O=C1c2cc(Br)ccc2CC1 SEQHEDQNODAFIU-UHFFFAOYSA-N 0.000 description 2
- XDRJVBDUUTZUAE-UHFFFAOYSA-N Bc1cc(OC)cc(C)c1 Chemical compound Bc1cc(OC)cc(C)c1 XDRJVBDUUTZUAE-UHFFFAOYSA-N 0.000 description 1
- KGKAYWMGPDWLQZ-UHFFFAOYSA-N BrCc1ccccc1CBr Chemical compound BrCc1ccccc1CBr KGKAYWMGPDWLQZ-UHFFFAOYSA-N 0.000 description 1
- RMWVUWLBLWBQDS-UHFFFAOYSA-N CC(C)(C)OC(CCBr)=O Chemical compound CC(C)(C)OC(CCBr)=O RMWVUWLBLWBQDS-UHFFFAOYSA-N 0.000 description 1
- OQJXZZLRSIISGJ-UHFFFAOYSA-N CC(C)(C)OC(CCN(C(C1(c2cc(C#CC3CC3)ccc2CC1(CC1)CCC1OC)N1)=O)C1=S)=[O]=C Chemical compound CC(C)(C)OC(CCN(C(C1(c2cc(C#CC3CC3)ccc2CC1(CC1)CCC1OC)N1)=O)C1=S)=[O]=C OQJXZZLRSIISGJ-UHFFFAOYSA-N 0.000 description 1
- ABZGJWWFJQRSDF-UHFFFAOYSA-N CC(C)(C)OC(CCN(C(c1cc(C#CC2CC2)ccc1CCCCC(CCCN1)OC)=O)C1=O)=O Chemical compound CC(C)(C)OC(CCN(C(c1cc(C#CC2CC2)ccc1CCCCC(CCCN1)OC)=O)C1=O)=O ABZGJWWFJQRSDF-UHFFFAOYSA-N 0.000 description 1
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- ZGMXAXRVEMIDBS-PBSMCPNCSA-N CN1C(N)=N[C@]2(c3cc(-c4cccc(Cl)c4)ccc3CC2(CC2)CCC2OC)C1=O Chemical compound CN1C(N)=N[C@]2(c3cc(-c4cccc(Cl)c4)ccc3CC2(CC2)CCC2OC)C1=O ZGMXAXRVEMIDBS-PBSMCPNCSA-N 0.000 description 1
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- HNFROVVMIDYSEZ-UHFFFAOYSA-N CN1OC2(c3cc(Br)ccc3CC2(CC2)CCC2OC)N=C1N Chemical compound CN1OC2(c3cc(Br)ccc3CC2(CC2)CCC2OC)N=C1N HNFROVVMIDYSEZ-UHFFFAOYSA-N 0.000 description 1
- RZSSUBGVLTWUMX-UHFFFAOYSA-N CN1OC2(c3cc(Br)ccc3CC22CCc3ccccc3CC2)N=C1N Chemical compound CN1OC2(c3cc(Br)ccc3CC22CCc3ccccc3CC2)N=C1N RZSSUBGVLTWUMX-UHFFFAOYSA-N 0.000 description 1
- ZBVLOFGSWBZQOS-UHFFFAOYSA-N COC(CC1)CCC1(Cc(c1c2)ccc2-c2cnc[s]2)C11N=C(N)N(Cc2ccccc2)C1=O Chemical compound COC(CC1)CCC1(Cc(c1c2)ccc2-c2cnc[s]2)C11N=C(N)N(Cc2ccccc2)C1=O ZBVLOFGSWBZQOS-UHFFFAOYSA-N 0.000 description 1
- HGVFLOGXSINYIY-UHFFFAOYSA-N COC(CC1)CCC1(Cc(c1c2)ccc2C#CC2CC2)C1(C(N1)=O)NC1=O Chemical compound COC(CC1)CCC1(Cc(c1c2)ccc2C#CC2CC2)C1(C(N1)=O)NC1=O HGVFLOGXSINYIY-UHFFFAOYSA-N 0.000 description 1
- JPUMMMXXSDGAJG-UHFFFAOYSA-N COC(CC1)CCC1(Cc(c1c2)ccc2C#CC2CC2)C1(C(N1)=O)NC1=S Chemical compound COC(CC1)CCC1(Cc(c1c2)ccc2C#CC2CC2)C1(C(N1)=O)NC1=S JPUMMMXXSDGAJG-UHFFFAOYSA-N 0.000 description 1
- GJLMZSIHQKOVQB-UHFFFAOYSA-N COC(CC1)CCC1(Cc(c1c2)ccc2C#CC2CC2)C11N=C(N)N(CCC(O)=O)C1=O Chemical compound COC(CC1)CCC1(Cc(c1c2)ccc2C#CC2CC2)C11N=C(N)N(CCC(O)=O)C1=O GJLMZSIHQKOVQB-UHFFFAOYSA-N 0.000 description 1
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- ZMGYJQUOCCHTCF-UHFFFAOYSA-N COC(CC1)CCC11/N=C(/N)\N(C2CC2)C2OC2c2cc([Br]=C)ccc2C1 Chemical compound COC(CC1)CCC11/N=C(/N)\N(C2CC2)C2OC2c2cc([Br]=C)ccc2C1 ZMGYJQUOCCHTCF-UHFFFAOYSA-N 0.000 description 1
- DCJRDHQOIROCOX-UHFFFAOYSA-N COC(CCCCc(c1c2)ccc2-c2cc(C(F)(F)F)cnc2)CCC/N=C(/N)\N(C2CC2)C1=O Chemical compound COC(CCCCc(c1c2)ccc2-c2cc(C(F)(F)F)cnc2)CCC/N=C(/N)\N(C2CC2)C1=O DCJRDHQOIROCOX-UHFFFAOYSA-N 0.000 description 1
- MKJBTAOROKUWJR-UILWBTOOSA-N CO[C@H](CC1)CC[C@]1(C(c1c2cc(CC3CCCCC3)cc1)=C)C2=O Chemical compound CO[C@H](CC1)CC[C@]1(C(c1c2cc(CC3CCCCC3)cc1)=C)C2=O MKJBTAOROKUWJR-UILWBTOOSA-N 0.000 description 1
- NMIRLXDILRJIMB-JSHSSLOESA-N CO[C@H](CC1)CC[C@]1(Cc(c1c2)ccc2OCc(cc2)ccc2OC)/C1=N/C#N Chemical compound CO[C@H](CC1)CC[C@]1(Cc(c1c2)ccc2OCc(cc2)ccc2OC)/C1=N/C#N NMIRLXDILRJIMB-JSHSSLOESA-N 0.000 description 1
- PYWMQUOIZBOVRE-UHFFFAOYSA-N COc1ccc(COc2ccc(CC(CC3)(CCC3=O)C3=O)c3c2)cc1 Chemical compound COc1ccc(COc2ccc(CC(CC3)(CCC3=O)C3=O)c3c2)cc1 PYWMQUOIZBOVRE-UHFFFAOYSA-N 0.000 description 1
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- HMIWEFCAUJPAMA-UHFFFAOYSA-N Cc(ccc(F)c1)c1-c1ccc(CC(CC2)(CCC2OC)C23ON(C)C(N)=N2)c3c1 Chemical compound Cc(ccc(F)c1)c1-c1ccc(CC(CC2)(CCC2OC)C23ON(C)C(N)=N2)c3c1 HMIWEFCAUJPAMA-UHFFFAOYSA-N 0.000 description 1
- BJQCPCFFYBKRLM-UHFFFAOYSA-N Cc1cc(B(O)O)ccc1 Chemical compound Cc1cc(B(O)O)ccc1 BJQCPCFFYBKRLM-UHFFFAOYSA-N 0.000 description 1
- FCZVBDJQRVNDRJ-UHFFFAOYSA-N Cc1n[n](C)c(CC2)c1CC2(Cc(c1c2)ccc2-c2cc(F)cc(Cl)c2)C11ON(C)C(N)=N1 Chemical compound Cc1n[n](C)c(CC2)c1CC2(Cc(c1c2)ccc2-c2cc(F)cc(Cl)c2)C11ON(C)C(N)=N1 FCZVBDJQRVNDRJ-UHFFFAOYSA-N 0.000 description 1
- MEBFBGRYWYRHBD-UHFFFAOYSA-N Cc1n[n](C)c(CC2)c1CC2(Cc(c1c2)ccc2Br)C11ON(C)C(N)=N1 Chemical compound Cc1n[n](C)c(CC2)c1CC2(Cc(c1c2)ccc2Br)C11ON(C)C(N)=N1 MEBFBGRYWYRHBD-UHFFFAOYSA-N 0.000 description 1
- XPJMRMFTIMDSAD-UHFFFAOYSA-N Fc1c(CCBr)cc(CBr)cc1 Chemical compound Fc1c(CCBr)cc(CBr)cc1 XPJMRMFTIMDSAD-UHFFFAOYSA-N 0.000 description 1
- CAEGHWMZYFLCBD-UHFFFAOYSA-N Fc1cc(CCBr)c(CBr)cc1 Chemical compound Fc1cc(CCBr)c(CBr)cc1 CAEGHWMZYFLCBD-UHFFFAOYSA-N 0.000 description 1
- XPUKSEWCOGRQQM-FCDQGJHFSA-N N#C/N=C1\c2cc(Br)ccc2CC11CCc2ccccc2CC1 Chemical compound N#C/N=C1\c2cc(Br)ccc2CC11CCc2ccccc2CC1 XPUKSEWCOGRQQM-FCDQGJHFSA-N 0.000 description 1
- CGFIGOOFLSBBHA-GNVQSUKOSA-N N#Cc1cc(-c2cc(/C(/C3(C4)Cc5ccccc5OCC3)=N/C#N)c4cc2)ccc1 Chemical compound N#Cc1cc(-c2cc(/C(/C3(C4)Cc5ccccc5OCC3)=N/C#N)c4cc2)ccc1 CGFIGOOFLSBBHA-GNVQSUKOSA-N 0.000 description 1
- SJZHYFNXQBSACR-UHFFFAOYSA-N O=C1c2cc(Br)ccc2CC1(CCc1c2)Cc1ccc2F Chemical compound O=C1c2cc(Br)ccc2CC1(CCc1c2)Cc1ccc2F SJZHYFNXQBSACR-UHFFFAOYSA-N 0.000 description 1
- DPMGNQWLPQTVPS-UHFFFAOYSA-N O=C1c2cc(Br)ccc2CC11Cc2ccccc2C1 Chemical compound O=C1c2cc(Br)ccc2CC11Cc2ccccc2C1 DPMGNQWLPQTVPS-UHFFFAOYSA-N 0.000 description 1
- VJQZLVZNOAKWKJ-UHFFFAOYSA-N O=Cc1ccccc1OCCCl Chemical compound O=Cc1ccccc1OCCCl VJQZLVZNOAKWKJ-UHFFFAOYSA-N 0.000 description 1
- SCWPNMHQRGNQHH-AATRIKPKSA-N OC(/C=C/c1ccccc1C(O)=O)=O Chemical compound OC(/C=C/c1ccccc1C(O)=O)=O SCWPNMHQRGNQHH-AATRIKPKSA-N 0.000 description 1
- DTQVDTLACAAQTR-UHFFFAOYSA-N OC(C(F)(F)F)=O Chemical compound OC(C(F)(F)F)=O DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 1
- VEEXBQLWMFMATJ-UHFFFAOYSA-N OC(CCc(cccc1)c1C(O)=O)=O Chemical compound OC(CCc(cccc1)c1C(O)=O)=O VEEXBQLWMFMATJ-UHFFFAOYSA-N 0.000 description 1
- RPAWLFZTBQQIDR-UHFFFAOYSA-N OCc1ccccc1OCCCl Chemical compound OCc1ccccc1OCCCl RPAWLFZTBQQIDR-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/12—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms condensed with carbocyclic rings or ring 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
- A61K31/41—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
- A61K31/4245—Oxadiazoles
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/28—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/44—Nitrogen atoms not forming part of a nitro radical
- C07D233/46—Nitrogen atoms not forming part of a nitro radical with only hydrogen atoms attached to said nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
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| US9725469B2 (en) | 2012-11-15 | 2017-08-08 | Amgen, Inc. | Amino-oxazine and amino-dihydrothiazine compounds as beta-secretase modulators and methods of use |
| US10550327B2 (en) | 2012-11-21 | 2020-02-04 | Merck Patent Gmbh | Polymerisable compounds and the use thereof in liquid-crystal displays |
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| BR112019025212A2 (pt) * | 2017-06-14 | 2020-06-16 | Nippon Soda Co., Ltd. | Composto, formulações para controlar organismos nocivos, para controlar ectoparasitas, para controlar pragas de insetos thysanoptera, e, formulação inseticida ou acaricida |
| KR101969528B1 (ko) | 2017-09-29 | 2019-04-16 | 에스케이텔레콤 주식회사 | 터치 디스플레이를 제어하는 장치와 방법 및 터치 디스플레이 시스템 |
| WO2019168874A1 (en) | 2018-02-27 | 2019-09-06 | The Research Foundation For The State University Of New York | Difluoromethoxylation and trifluoromethoxylation compositions and methods for synthesizing same |
| CN108675922B (zh) * | 2018-06-27 | 2021-04-27 | 沅江华龙催化科技有限公司 | 一种螺环化合物及其合成方法 |
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