KR860003217A - 복소환식 아미드의 제법 - Google Patents
복소환식 아미드의 제법 Download PDFInfo
- Publication number
- KR860003217A KR860003217A KR1019850007730A KR850007730A KR860003217A KR 860003217 A KR860003217 A KR 860003217A KR 1019850007730 A KR1019850007730 A KR 1019850007730A KR 850007730 A KR850007730 A KR 850007730A KR 860003217 A KR860003217 A KR 860003217A
- Authority
- KR
- South Korea
- Prior art keywords
- formula
- alkyl
- compound
- alkoxy
- optionally
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- 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
-
- 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
- A61P9/08—Vasodilators for multiple indications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/12—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/82—Carbazoles; Hydrogenated carbazoles
- C07D209/88—Carbazoles; Hydrogenated carbazoles 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 carbon atoms of the ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
- C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
- C07D401/02—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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Rheumatology (AREA)
- Cardiology (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Immunology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Pyrrole Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Steroid Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Peptides Or Proteins (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (20)
- (a) Ri가 임의로, 아세톡시, (1-4C)알콕시 또는 (1-C)알킬티오 치환체를 갖는 (1-6C)알킬, 또는 페닐 또는 벤질인 구조식(5)의 적당한 에스테르를 분해하여 Z가 카복실산 그룹인 구조식(1)
-
- 의 화합물로 만들고; (b) 구조식(6)의 아민을 아실화하여,
-
- Re, Lo1 Re.X.CO.NH- 또는 Re.X.CS.NH- 그룹인 구조식(1)의 화합물로 만들고; (c) A가 -CH= 또는 -N=인 구조식(7)의 인돌 또는 인다졸 유도체를
-
- U가 적당한 이탈기인 구조식(8)의 알킬화제와 반응시켜,
-
- A.CRa가 디래디칼 -CRb=CRa- 또는 -N-CRa인 구조식(1)의 화합물로 만들고; (d) 구조식(9)의 시아노 유도체를 아지와 반응시켜,
-
- Z가 1(H)-테트라졸-5-일 래디칼인 구조식(1)의 화합물로 만들고; (e) Ra가 수소인 구조식(1)의 화합물을 할로겐하여, Ra가 할노게노인 구조식(1)의 화합물로 만들고; (f) Xb가 산소 또는 황인 구조식(10)의 이소시아네이트 또는 이소티오시아네이트를 Re,XH의 적당한 화합물과 반응시켜
-
- Re.L Re. X. CO. NH- 또는 Re. X. CS. NH-이고 X가 옥시 또는 티오인 구조식(1)의 화합물로 만들고; (g) Z가 카복시인 구조식(1)의 화합물을 Rg. SOnNH2의 설폰아미드 유도체와 반응시켜, Z가 -CO. NH. SOn. Rg인 구조식(1)의 화합물로 만들고; (h) Ra가 ((1-6C)알콕시)카보닐 및/또는 ((1-6C)알콜시카보닐-(1-3C))알킬 또는 ((1-6C)알콜시카보닐페닐)메틸을 가지는 구조식(1)의 에스테르를 분해하여, Ra가 카복시 치환제를 가지고 및/또는 Rh가 카복시-(1-3C)알킬 또는 (카복시페닐메틸인 구조식(1)의 상응하는 화합물로 만들고; (i) Xb가 옥시 또는 티오인 구조식(1)의 화합물을
-
- 이소시아네이트 유도체 ONC. SOn. Ra와 반응시켜, Z가 아실설폰아미드인 CO. NH. SOn. Rg그룹이고 G2가 Z에 직접 결합하고 Q가 산소 또는 황인 구조식(1)의 화합물로 만들고, (j) Z가 CO. NH. SO. Rg 그룹인 구조식(1)의 아실설핀아미드를 산화하여, Z가 CO. NH. SOn. Rg의 아실설폰아미드그룹인 구조식(1)의 상응하는 화합물로 만들고 (k) Ra가 임의로 카복시 또는 ((1-4C)알콕시)카보닐 치환제를 가지는 (2-6C)알케닐인 구조식(1)의 화합물을 환원하여, Ra가 임의로 카복시 또는 ((1-4C)알콕시)카보닐 치환체를 가지는 (2-6C)알킬인 구조식(1)의 화합물로 만드는; 것을 특징으로 하는 구조식(1)의 아미드 화합물을 제조하는 방법.
-
- [식중, A CRa는 -CRb=CRa-, -CHRb, CHRa- 및 -N=CRa-의 디래디칼에서 선택 Ra는 수소, 메틸, 할로게노, (2-6C)알카노일 임의로 카복시 또는 ((1-4C)알콕시)카보닐 치환제를 가지는 (2-6C)알케닐 또는 (2-6C)알킬 Rb는 수소 또는 (1-4C)알킬 또는 Ra 및 Rb는 임의로 1 또는 2(1-4C)알킬 치환제 및 임의로 1 또는 그 불포화결합을 포함하는 테트라메틸렌을 함께 형성 Rc,Rd 및 Rf는 수소, 할로게노(1-4C)알킬 및 (1-4C)알콕시에서 독립적으로 선택, Re. L은 벤지노이드환의 4,5 또는 6위치에 부착된 Ce. X. CO. NH-, Re. X. CS. NH- 또는 Re. NH. CO-의 아미드 래디칼, Re는 1 또는 그 이상의 불소치환제를 임의로 포함하는 (2-10C)알킬; (3-10C)알케닐 또는 (3-10C)알키닐, (1-6C)알킬부분은 (1-4C)알콕시, (3-6C)싸이클로알킬 또는 페닐치환제를 임의로 포함하고, 페닐 또는 티에닐부분은 할로게노, (1-4C)알킬, (1-4C)알콕시 및 트리플루오로메틸에서 선택된 1 또는 2치환제를 임의로 포함하는 페닐, 페닐-(1-6C)알킬 또는 티에닐-(1-6C)알킬; 싸이클 부분은 하나의 불포화결합 또는 1 또는 2(1-4C)알킬치환제 또는 페닐치환제를 포함하고, 페닐치환제는 할로게노, (1-4C)알킬, (1-4C)알콕시 또는 트리플루오로메틸 치환제를 임의로 갖는 (3-8C)싸이클로알킬, (3-8C)싸이클로알킬-(1-6C)알킬 또는 (4-6C)옥시헤테로싸이클릴, X는 옥시, 티오, 아미노 또는 Re에 직접결합, Q는 G1에 직접결합 또는 옥시, 티오, m-페닐렌, p-페닐렌 또는 헤테로아릴렌, G1은 (1-8C)알킬렌 또는 (2-6C)알케닐렌 G2는 메틸렌, 비틸렌 또는 Z에 직접결합, Z는 n이 1 또는 그이고 Rg가 방향족 또는 헤테로방향족 부분은 할로게노, (1-4C)알킬(1-4C)알콕시, 트리플루오로메틸, 니트로 및 아미노에서 독립적으로 선택된 1 또는 2치환제를 임의로 포함하는 (1-6C)알킬, 아릴, 헤테로아릴, 아릴-(1-4C)알킬이고 Rh는 수소, 카복시-(1-3C)알킬 또는 (카복시페닐)메틸인-CO.NH. SOn. Rg의 알실설폰아미드 잔사, 구조식(2)의 테트라졸릴 및 카복시에서 선택된 산성그룹.
-
- Q가 옥시 또는 티오 및 Z가 카복시일 때 G2가 메틸렌 또는 비닐렌이고, G1.Q 및 G2는 최소한 3탄소원자를 함께 포함.]
- ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB848426474A GB8426474D0 (en) | 1984-10-19 | 1984-10-19 | Heterocyclic amides |
GB8426474 | 1984-10-19 | ||
GB8507305 | 1985-03-21 | ||
GB858507305A GB8507305D0 (en) | 1985-03-21 | 1985-03-21 | Amide derivatives |
GB858507861A GB8507861D0 (en) | 1985-03-26 | 1985-03-26 | Carboxylic acid derivatives |
GB8507861 | 1985-03-26 | ||
GB8507862 | 1985-03-26 | ||
GB858507862A GB8507862D0 (en) | 1985-03-26 | 1985-03-26 | Carboxamides |
Publications (2)
Publication Number | Publication Date |
---|---|
KR860003217A true KR860003217A (ko) | 1986-05-21 |
KR900007419B1 KR900007419B1 (ko) | 1990-10-08 |
Family
ID=27449596
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019850007730A KR900007419B1 (ko) | 1984-10-19 | 1985-10-19 | 복소환식 아미드 및 그 제조방법 |
Country Status (20)
Country | Link |
---|---|
US (1) | US4997844A (ko) |
EP (1) | EP0179619B1 (ko) |
JP (1) | JPH0745466B2 (ko) |
KR (1) | KR900007419B1 (ko) |
CN (1) | CN85108623A (ko) |
AT (1) | ATE56205T1 (ko) |
CA (1) | CA1273934A (ko) |
DE (1) | DE3579554D1 (ko) |
DK (1) | DK169541B1 (ko) |
ES (5) | ES8704458A1 (ko) |
FI (1) | FI854024L (ko) |
GB (1) | GB8524157D0 (ko) |
GR (1) | GR852519B (ko) |
HU (1) | HU194163B (ko) |
IE (1) | IE58848B1 (ko) |
IL (1) | IL76756A (ko) |
NO (1) | NO854163L (ko) |
NZ (1) | NZ213872A (ko) |
PT (1) | PT81297B (ko) |
ZW (1) | ZW18185A1 (ko) |
Families Citing this family (63)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8623429D0 (en) * | 1985-10-17 | 1986-11-05 | Ici America Inc | Carboximide derivatives |
EP0227241B1 (en) * | 1985-10-17 | 1996-09-11 | Zeneca Inc. | Medicinal indole and indazole keto sulphone derivatives |
GB8609175D0 (en) * | 1986-04-15 | 1986-05-21 | Ici America Inc | Heterocyclic carboxamides |
GB8707051D0 (en) * | 1986-04-15 | 1987-04-29 | Ici America Inc | Heterocyclic carboxamides |
MY103259A (en) * | 1987-04-15 | 1993-05-29 | Ici America Inc | Aliphatic carboxamides |
US4894386A (en) * | 1987-04-15 | 1990-01-16 | Ici Americas Inc. | Aliphatic carboxamides |
GB8807275D0 (en) * | 1988-03-26 | 1988-04-27 | Synphar Lab Inc | Chemical compounds |
CA1337202C (en) * | 1988-04-13 | 1995-10-03 | Victor Giulio Matassa | Cyclic amides which are leukotriene antagonists |
US5047402A (en) * | 1988-04-13 | 1991-09-10 | Ici Americas Inc. | Cyclic amides as medicaments |
US5095038A (en) * | 1988-04-14 | 1992-03-10 | Ici Americas Inc. | Carbocyclic compounds useful as leukotriene antagonists |
GB8906032D0 (en) * | 1988-04-14 | 1989-04-26 | Ici America Inc | Hetera-aliphatic carboxamides |
US5041460A (en) * | 1988-04-14 | 1991-08-20 | Ici Americas Inc. | Heter-aliphatic carboxamides |
ZA892643B (en) * | 1988-04-14 | 1989-12-27 | Ici America Inc | Carbocyclic compounds |
US5281593A (en) * | 1990-07-31 | 1994-01-25 | Lilly Industries Limited | Certain indole derivatives useful as leukotriene antagonists |
AU654140B2 (en) * | 1990-07-31 | 1994-10-27 | Lilly Industries Limited | N-benzyl indoles, processes for their preparation or pharmaceutical compositions containing them |
GB9020338D0 (en) * | 1990-09-18 | 1990-10-31 | Lilly Industries Ltd | Pharmaceutical compounds |
US5334597A (en) * | 1991-10-17 | 1994-08-02 | Merck Frosst Canada, Inc. | Indole carbamates as leukotriene antagonists |
US5217983A (en) * | 1992-03-27 | 1993-06-08 | Du Pont Merck Pharmaceutical Company | (N-benzyl) acetaldehyde bicyclic heterocycles useful as topical antiinflammatories |
US5272169A (en) * | 1992-03-27 | 1993-12-21 | The Dupont Merck Pharmaceutical Company | (N-benzyl) acetaldehyde bicyclic heterocycles useful as topical antiinflammatories |
US5439929A (en) * | 1994-03-01 | 1995-08-08 | Pfizer Inc. | Bicyclic carbamates, pharmaceutical compositions and use |
CA2264798A1 (en) * | 1996-09-04 | 1998-03-12 | Pfizer Inc. | Indazole derivatives and their use as inhibitors of phosphodiesterase (pde) type iv and the production of tumor necrosis factor (tnf) |
GB9919413D0 (en) | 1999-08-18 | 1999-10-20 | Zeneca Ltd | Chemical compounds |
GB9919411D0 (en) * | 1999-08-18 | 1999-10-20 | Zeneca Ltd | Chemical compounds |
JP4955171B2 (ja) * | 1999-11-16 | 2012-06-20 | ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド | 抗炎症剤としての尿素誘導体 |
GB0010757D0 (en) | 2000-05-05 | 2000-06-28 | Astrazeneca Ab | Chemical compounds |
CA2432008A1 (en) * | 2000-12-22 | 2002-07-04 | Astrazeneca Ab | Carbazole derivatives and their use as neuropeptide y5 receptor ligands |
GB0121941D0 (en) | 2001-09-11 | 2001-10-31 | Astrazeneca Ab | Chemical compounds |
US20050124620A1 (en) * | 2002-04-09 | 2005-06-09 | Martyn Frederickson | Pharmaceutical compounds |
US7135575B2 (en) * | 2003-03-03 | 2006-11-14 | Array Biopharma, Inc. | P38 inhibitors and methods of use thereof |
CN101263121A (zh) | 2005-07-14 | 2008-09-10 | 塔克达圣地亚哥公司 | 组蛋白脱乙酰基酶抑制剂 |
EP1919866A2 (en) | 2005-08-17 | 2008-05-14 | Wyeth a Corporation of the State of Delaware | Substituted indoles and use thereof |
UA94733C2 (ru) * | 2006-01-31 | 2011-06-10 | Эррей Биофарма Инк. | Ингибиторы киназы и способы их использования |
MX2008010645A (es) * | 2006-02-20 | 2008-10-14 | Astellas Pharma Inc | Derivado de amida o sal del mismo. |
EP2007756B1 (en) | 2006-04-07 | 2015-08-26 | Vertex Pharmaceuticals Incorporated | Modulators of atp-binding cassette transporters |
US10022352B2 (en) | 2006-04-07 | 2018-07-17 | Vertex Pharmaceuticals Incorporated | Modulators of ATP-binding cassette transporters |
US7645789B2 (en) | 2006-04-07 | 2010-01-12 | Vertex Pharmaceuticals Incorporated | Indole derivatives as CFTR modulators |
US8563573B2 (en) | 2007-11-02 | 2013-10-22 | Vertex Pharmaceuticals Incorporated | Azaindole derivatives as CFTR modulators |
US8802868B2 (en) | 2010-03-25 | 2014-08-12 | Vertex Pharmaceuticals Incorporated | Solid forms of (R)-1(2,2-difluorobenzo[D][1,3]dioxo1-5-yl)-N-(1-(2,3-dihydroxypropyl-6-fluoro-2-(1-hydroxy-2-methylpropan2-yl)-1H-Indol-5-yl)-Cyclopropanecarboxamide |
MX342288B (es) | 2010-04-22 | 2016-09-23 | Vertex Pharma | Proceso para producir compuestos de cicloalquilcarboxamido-indol. |
US8957093B2 (en) | 2011-06-06 | 2015-02-17 | The Scripps Research Institute | N-biphenylmethylindole modulators of PPARG |
US9051265B2 (en) | 2011-06-06 | 2015-06-09 | The Scripps Research Institute | N-benzylindole modulators of PPARG |
WO2013064984A1 (en) | 2011-10-31 | 2013-05-10 | Xenon Pharmaceuticals Inc. | Biaryl ether sulfonamides and their use as therapeutic agents |
US9630929B2 (en) | 2011-10-31 | 2017-04-25 | Xenon Pharmaceuticals Inc. | Benzenesulfonamide compounds and their use as therapeutic agents |
WO2013078240A1 (en) | 2011-11-22 | 2013-05-30 | Ripka Amy S | N-biphenylmethylbenzimidazole modulators of pparg |
EP2844259A4 (en) | 2012-04-30 | 2015-11-11 | Anderson Gaweco | MMR MODULATORS AND USES THEREOF |
EA026393B1 (ru) * | 2012-05-22 | 2017-04-28 | Дженентек, Инк. | N-замещенные бензамиды и их применение в лечении боли |
KR101663436B1 (ko) | 2012-07-06 | 2016-10-06 | 제넨테크, 인크. | N-치환된 벤즈아미드 및 이의 사용 방법 |
US9012496B2 (en) | 2012-07-16 | 2015-04-21 | Vertex Pharmaceuticals Incorporated | Pharmaceutical compositions of (R)-1-(2,2-difluorobenzo[D][1,3]dioxol-5-yl)-N-(1-(2,3-dihydroxypropyl)-6-fluoro-2-(1-hydroxy-2-methylpropan-2-yl)-1H-indol-5-yl)cyclopropanecarboxamide and administration thereof |
EP2968280A4 (en) | 2013-03-14 | 2016-08-10 | Genentech Inc | SUBSTITUTED TRIAZOLOPYRIDINES AND METHOD OF USE THEREOF |
WO2014144545A2 (en) | 2013-03-15 | 2014-09-18 | Genentech, Inc. | Substituted benzoxazoles and methods of use thereof |
EP3450428A1 (en) | 2013-11-27 | 2019-03-06 | Genentech, Inc. | Substituted benzamides and methods of use thereof |
ES2957761T3 (es) | 2014-04-15 | 2024-01-25 | Vertex Pharma | Composiciones farmacéuticas para el tratamiento de enfermedades mediadas por el regulador de la conductancia transmembrana de fibrosis quística |
US10016394B2 (en) | 2014-04-16 | 2018-07-10 | The Scripps Research Institute | PPARG modulators for treatment of osteoporosis |
US10005724B2 (en) | 2014-07-07 | 2018-06-26 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
KR20180008761A (ko) | 2015-05-22 | 2018-01-24 | 제넨테크, 인크. | 치환된 벤즈아미드 및 이의 이용 방법 |
WO2017035271A1 (en) | 2015-08-27 | 2017-03-02 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
CA2999769A1 (en) | 2015-09-28 | 2017-04-06 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
EP3380466A1 (en) | 2015-11-25 | 2018-10-03 | Genentech, Inc. | Substituted benzamides useful as sodium channel blockers |
JP2019513714A (ja) | 2016-03-30 | 2019-05-30 | ジェネンテック, インコーポレイテッド | 置換ベンズアミド及びその使用方法 |
CA3039853A1 (en) | 2016-10-17 | 2018-04-26 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
JP2020511511A (ja) | 2017-03-24 | 2020-04-16 | ジェネンテック, インコーポレイテッド | ナトリウムチャネル阻害剤としての4−ピペリジン−n−(ピリミジン−4−イル)クロマン−7−スルホンアミド誘導体 |
TW202000651A (zh) | 2018-02-26 | 2020-01-01 | 美商建南德克公司 | 治療性組成物及其使用方法 |
CN111936494A (zh) | 2018-03-30 | 2020-11-13 | 豪夫迈·罗氏有限公司 | 作为钠通道抑制剂的取代的氢-吡啶并-吖嗪 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AT234103B (de) * | 1959-09-03 | 1964-06-10 | Merck & Co Inc | Verfahren zur Herstellung von neuen, benzylindolylsubstituierten niedrigen aliphatischen Säuren sowie deren Salzen und Estern |
US3271416A (en) * | 1961-10-24 | 1966-09-06 | Merck & Co Inc | Indolyl aliphatic acids |
FR4035M (ko) * | 1964-11-04 | 1966-03-28 | ||
FR5000M (ko) * | 1965-06-12 | 1967-04-17 | ||
IT7920398A0 (it) * | 1979-02-21 | 1979-02-21 | Resfar Srl | Derivato ad attivita' analgesica antiinfiammatoria potenziata eprocedimento per la sua preparazione. |
US4363912A (en) * | 1980-12-15 | 1982-12-14 | Pfizer Inc. | Indole thromboxane synthetase inhibitors |
GB2111050B (en) * | 1981-11-19 | 1985-09-11 | Ciba Geigy Ag | N-substituted-2-pyridylindoles |
IE54269B1 (en) * | 1981-12-30 | 1989-08-02 | Ici America Inc | Pharmaceutically active phenylcarboxylic acid derivatives |
DE4138853A1 (de) * | 1991-11-27 | 1993-06-03 | Bayer Ag | 5,6-dihydro-dibenz(b,e)azepin-6,11-dion-11- oxime |
-
1985
- 1985-10-01 GB GB858524157A patent/GB8524157D0/en active Pending
- 1985-10-14 PT PT81297A patent/PT81297B/pt not_active IP Right Cessation
- 1985-10-16 FI FI854024A patent/FI854024L/fi not_active Application Discontinuation
- 1985-10-16 HU HU854007A patent/HU194163B/hu not_active IP Right Cessation
- 1985-10-17 DE DE8585307498T patent/DE3579554D1/de not_active Expired - Fee Related
- 1985-10-17 AT AT85307498T patent/ATE56205T1/de not_active IP Right Cessation
- 1985-10-17 ZW ZW181/85A patent/ZW18185A1/xx unknown
- 1985-10-17 EP EP85307498A patent/EP0179619B1/en not_active Expired - Lifetime
- 1985-10-17 NZ NZ213872A patent/NZ213872A/xx unknown
- 1985-10-18 JP JP60231457A patent/JPH0745466B2/ja not_active Expired - Fee Related
- 1985-10-18 DK DK479385A patent/DK169541B1/da not_active IP Right Cessation
- 1985-10-18 GR GR852519A patent/GR852519B/el unknown
- 1985-10-18 ES ES548011A patent/ES8704458A1/es not_active Expired
- 1985-10-18 US US06/788,807 patent/US4997844A/en not_active Expired - Lifetime
- 1985-10-18 CA CA000493372A patent/CA1273934A/en not_active Expired - Lifetime
- 1985-10-18 IE IE258985A patent/IE58848B1/en not_active IP Right Cessation
- 1985-10-18 NO NO854163A patent/NO854163L/no unknown
- 1985-10-18 IL IL76756A patent/IL76756A/xx not_active IP Right Cessation
- 1985-10-19 KR KR1019850007730A patent/KR900007419B1/ko not_active IP Right Cessation
- 1985-10-19 CN CN198585108623A patent/CN85108623A/zh active Pending
-
1986
- 1986-04-30 ES ES554578A patent/ES8800900A1/es not_active Expired
- 1986-04-30 ES ES554577A patent/ES8800899A1/es not_active Expired
- 1986-04-30 ES ES554580A patent/ES8801786A1/es not_active Expired
- 1986-04-30 ES ES554579A patent/ES8802495A1/es not_active Expired
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR860003217A (ko) | 복소환식 아미드의 제법 | |
ES8801787A1 (es) | Procedimiento para la obtencion de amidas de acidos benzoheterociclilalcanoicos | |
AU3273289A (en) | Indolyl and indazolyl cyclic amides | |
NZ228722A (en) | Substituted indole and indazole derivatives and pharmaceutical compositions | |
IE862737L (en) | Heterocyclic compounds | |
MY103259A (en) | Aliphatic carboxamides | |
DE2709634A1 (de) | Benzylpyrimidine, verfahren zu ihrer herstellung und diese enthaltende arzneimittel | |
KR960704889A (ko) | 인돌리진 유도체의 제조방법 (Process for the preparation of indolizine derivatives) | |
EP0082648A2 (en) | Cephalosporin derivatives | |
JPS61289079A (ja) | マロン酸誘導体 | |
TH30743EX (th) | อนุพันธ์ 3-อามิโดโพราโซล ขบวนการสำหรับเตรียมและองค์ประกอบเภสัชกรรมที่ประกอบด้วยสารดังกล่าว |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
E902 | Notification of reason for refusal | ||
E902 | Notification of reason for refusal | ||
G160 | Decision to publish patent application | ||
E701 | Decision to grant or registration of patent right | ||
GRNT | Written decision to grant | ||
LAPS | Lapse due to unpaid annual fee |