KR950032184A - 3-(2-아미노에틸)-4-[3-(트리플루오로메틸)벤조일]-3, 4-디히드로-2h-1, 4-벤즈옥사진 유도체, 그 제조방법 및 그 치료학적 적용 - Google Patents

3-(2-아미노에틸)-4-[3-(트리플루오로메틸)벤조일]-3, 4-디히드로-2h-1, 4-벤즈옥사진 유도체, 그 제조방법 및 그 치료학적 적용 Download PDF

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KR950032184A
KR950032184A KR1019950001835A KR19950001835A KR950032184A KR 950032184 A KR950032184 A KR 950032184A KR 1019950001835 A KR1019950001835 A KR 1019950001835A KR 19950001835 A KR19950001835 A KR 19950001835A KR 950032184 A KR950032184 A KR 950032184A
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group
dihydro
compound
general formula
inden
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KR1019950001835A
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조르쥬 빠스칼
프로스트 죠나단
빠쏘 빠트릭
루쎌 꼬린느
바르트쉬 레진느
하워드 윌리엄스 폴
끌로드 뮐레 쟝
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에. 뚜레 레메뜨르
신떼라보 소시에떼 아노님
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Priority claimed from FR9401196A external-priority patent/FR2715659B1/fr
Priority claimed from FR9401197A external-priority patent/FR2715655B1/fr
Application filed by 에. 뚜레 레메뜨르, 신떼라보 소시에떼 아노님 filed Critical 에. 뚜레 레메뜨르
Publication of KR950032184A publication Critical patent/KR950032184A/ko

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/06Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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    • C07D265/281,4-Oxazines; Hydrogenated 1,4-oxazines
    • C07D265/341,4-Oxazines; Hydrogenated 1,4-oxazines condensed with carbocyclic rings
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    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems

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Abstract

본 발명은 일반식(Ⅰ)에 해당하는 화합물을 제공한다.
상기식에서 R1은 수소원자, 플루오르원자, 염소원자, 메틸기, C1-C3알콕시기 또는 니트로기를 나타내며, R3는 수소원자 또는 C1-C3알킬기를 나타내며, R4는 2, 3-이히드로-1H-인덴-2-일, 2, 3-디히드로-1H-일 또는 1, 2, 3, 4-테트라히들고 나프탈렌-1-일기를 나타내거나 양자택일로 R3및 R4는 질소원자와 함께 1, 2, 3, 4-테트라히드로-9H-피리도[3,4-b]인돌-2-일기, 1, 2, 3, 4-테트라히드로-9H-피리도[4, 3-b]인돌-3-일기, 4, 5, 6, 7-테트라히드로티에노[2, 3-c]피리드-6-일기, 4, 5, 6, 7-테트라히드로티에노[3, 2-c]피리드-6-일기 또는 2, 3-디히드로-1H-이소인돌-2-일기를 형성한다.

Description

3-(2-아미노에틸)-4-[3-(트리플루오로메틸)벤조일]-3,4-디히드로-2H-1,4-벤즈옥사진 유도체, 그 제조방법 및 그 치료학적 적용
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (5)

  1. 염기의 형태 또는 산의 부가염 형태로 다음 일반식(I)에 해당하는 순수한 광학 이성질체 또는 광학 이성질체의 혼합물의 형태인 것을 특징으로 하는 화합물.
    상기식에서 R1은 수소원자, 플루오르원자, 염소원자, 메틸기, C1-C3알콕시기 또는 니트로기를 나타내며, R3는 단독으로 수소원자 또는 C1-C3알킬기를 나타내며, R4는 단독으로 2,3-디히드로-1H-인덴-2-일기, 2,3-디히드로-1H-인덴-1-일기 또는 1,2,3,4-테트라히드로 나프탈렌-1-일기를 나타내거나 또는 양자택일로, R3및 R4는 질소원자와 함께 1,2,3,4-테트라히드로-9H-피리도[3,4-b]인돌-2-일기, 1,2,3,4-테트라히드로-9H-피리도[4,3-b]인돌-3-일기, 4,5,6,7-테트라히드로티에노[2,3-c]피리드-6-일기, 4,5,6,7-테트라히드로티에노[3,2-c]피리드-6-일기 또는 2,3-디히드로-1H-이소인돌-2-일기를 함께 형성하며, 이들의 구조식은 각각 다음과 같다;
  2. 제1항에 있어서, R1은 플루오르원자, 염소원자, 메틸기 또는 메톡시기를 나타내며, R3는 수소원자 또는 C1-C3알킬기를 나타내며 R4는 2, 3-디히드로-1H-인덴-2-일기, 2, 3-디히드로-1H-인덴-1-일기 또는 1, 2, 3, 4-테트라히드로나프탈렌-1-일기를 나타내는 것을 특징으로 하는 화합물.
  3. R1의 특허청구의 번위 제1항에 정의된 바와 같은 일반식(Ⅱ)
    의 2-아미노페놀을 무수트리플루오로아세트산과 반응시켜서 일반식(Ⅳ)
    의 아미드를 얻고 이것을 에틸 4-브로모-2부텐오에이트와 반응시키고 이어서 그렇게 하여 얻어진 일반식(Ⅵ)
    의 에틸 3, 4-디히드로-2H-1, 4-벤즈옥사진-3-아세테이트 유도체의 에스테르 작용기를 환원제로 환원시켜서 일반식(Ⅶ)
    의 3, 4-디히드로-2H-1, 4-벤즈옥사진-3-에탄올 유도체를 얻고 이것을 3-(트리플루오로메틸)벤조일클로라이드와 반응시켜서 일반식(Ⅸ)
    의 알코올을 얻고 이것을 염화티오닐과 반응시켜서 일반식(Ⅹ)
    의 화합물을 얻고 최종적으로 이 화합물을 R3및 R4가 특허청의 범위 제1항에 규정된 바의 일반식 HNR3R4의 아민과 반응시키는 것을 특징으로 하는 특허청구의 범위 제1항에 따른 화합물의 제조방법.
  4. 특허청구의 범위 제1항에 따른 화합물로 구성되는 것을 특징으로 하는 약제.
  5. 특허청구의 범위 제1항에 따른 화합물을 부형제와 결합하여 함유하는 것을 특징으로 하는 약학적 조성물.
    ※ 참고사항 : 최초출원내용에 의하여 공개하는 것임.
KR1019950001835A 1994-02-03 1995-02-02 3-(2-아미노에틸)-4-[3-(트리플루오로메틸)벤조일]-3, 4-디히드로-2h-1, 4-벤즈옥사진 유도체, 그 제조방법 및 그 치료학적 적용 KR950032184A (ko)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
FR9401196A FR2715659B1 (fr) 1994-02-03 1994-02-03 Dérivés de 3-(2-aminoéthyl)-4-[3-(trifluorométhyl)benzoyl]-3,4-dihydro-2H-1,4-benzoxazine, leur préparation et leur application en thérapeutique.
FR94.01196 1994-02-03
FR94.01197 1994-02-03
FR9401197A FR2715655B1 (fr) 1994-02-03 1994-02-03 Dérivés de 3-(2-aminoéthyl)-4-benzoyl-3,4-dihydro-2H-1,4-benzoxazine, leur préparation et leur application en thérapeutique.

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KR950032184A true KR950032184A (ko) 1995-12-20

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EP (1) EP0666260B1 (ko)
JP (1) JPH07278123A (ko)
KR (1) KR950032184A (ko)
CN (1) CN1109880A (ko)
AT (1) ATE182887T1 (ko)
AU (1) AU687134B2 (ko)
CA (1) CA2141728A1 (ko)
CZ (1) CZ27095A3 (ko)
DE (1) DE69511127D1 (ko)
FI (1) FI950457A (ko)
HU (1) HUT71238A (ko)
IL (1) IL112528A (ko)
NO (1) NO304229B1 (ko)
NZ (1) NZ270444A (ko)
PL (1) PL307040A1 (ko)
RU (1) RU2136670C1 (ko)
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ZA (1) ZA95834B (ko)

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Publication number Priority date Publication date Assignee Title
ES2235368T3 (es) * 1997-10-27 2005-07-01 Sumitomo Pharmaceuticals Company, Limited Derivados de amida para tratar alteraciones neurodegenerativas de la retina.
JP3201998B2 (ja) * 1998-12-16 2001-08-27 サムソン ジェネラル ケミカルズ カンパニー リミテッド (s)−ベンゾオキサジン誘導体の製造方法及び(r)−ベンゾオキサジン誘導体のラセミ化方法
KR100397491B1 (ko) * 2000-12-05 2003-09-13 이수화학 주식회사 광학활성 (s)-벤즈옥사진 유도체 및 그의 제조방법
EP1856126A2 (en) * 2005-02-17 2007-11-21 Wyeth a Corporation of the State of Delaware Cycloalkylfused indole, benzothiophene, benzofuran and indene derivatives
CN101268075A (zh) * 2005-07-28 2008-09-17 百时美施贵宝公司 作为5-羟色胺受体激动剂和拮抗剂的取代的四氢-1h吡啶并[4,3,b]吲哚
AP2013007153A0 (en) 2011-03-18 2013-09-30 Lupin Ltd Benzo [B] [1,4] oxazin derivatives as calcium sensing receptor modulators

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1287584B (de) * 1962-07-04 1969-01-23 Thomae Gmbh Dr K Verfahren zur Herstellung von 2, 3-Dihydro-1, 4-benzoxazinderivaten
US4636563A (en) * 1985-09-16 1987-01-13 American Home Products Corporation Antipsychotic γ-carbolines
FR2619111B1 (fr) * 1987-08-07 1991-01-11 Synthelabo Derives de (piperidinyl-4)methyl-2 tetrahydro-1,2,3,4 9h-pyrido (3,4-b) indole, leur preparation et leur application en therapeutique
FR2702477B1 (fr) * 1993-03-08 1995-04-28 Synthelabo Dérivés de benzoxazine, leur préparation et leur application en thérapeutique.

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CZ27095A3 (en) 1995-09-13
ATE182887T1 (de) 1999-08-15
NO304229B1 (no) 1998-11-16
RU2136670C1 (ru) 1999-09-10
CN1109880A (zh) 1995-10-11
NZ270444A (en) 1996-02-27
IL112528A (en) 1999-04-11
RU95101386A (ru) 1996-11-20
EP0666260B1 (fr) 1999-08-04
IL112528A0 (en) 1995-05-26
FI950457A (fi) 1995-08-04
JPH07278123A (ja) 1995-10-24
NO950378D0 (no) 1995-02-02
AU687134B2 (en) 1998-02-19
NO950378L (no) 1995-08-04
SK12895A3 (en) 1995-08-09
ZA95834B (en) 1996-02-12
HUT71238A (en) 1995-11-28
PL307040A1 (en) 1995-08-07
US5550125A (en) 1996-08-27
EP0666260A1 (fr) 1995-08-09
HU9500310D0 (en) 1995-03-28
CA2141728A1 (en) 1995-08-04
DE69511127D1 (de) 1999-09-09
AU1154595A (en) 1995-08-10
FI950457A0 (fi) 1995-02-02

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