KR920012029A - 3위치에 치환된 인돌(indole)의 신규의 제조방법 및 본 방법에서 유용한 중간체 - Google Patents

3위치에 치환된 인돌(indole)의 신규의 제조방법 및 본 방법에서 유용한 중간체 Download PDF

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KR920012029A
KR920012029A KR1019910022262A KR910022262A KR920012029A KR 920012029 A KR920012029 A KR 920012029A KR 1019910022262 A KR1019910022262 A KR 1019910022262A KR 910022262 A KR910022262 A KR 910022262A KR 920012029 A KR920012029 A KR 920012029A
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acetaldehyde
nitrophenyl
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톰스 쟈콥스 로버트
프란시스 코스텔로 제라드
아란 브룩 스테펜
존 하리슨 페터
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수잔 제인 젠틀
임페리얼 케미칼 인더스트리스 피엘씨
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/18Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D209/24Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with an alkyl or cycloalkyl radical attached to the ring nitrogen atom
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    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C201/00Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
    • C07C201/06Preparation of nitro compounds
    • C07C201/12Preparation of nitro compounds by reactions not involving the formation of nitro groups
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    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C227/04Formation of amino groups in compounds containing carboxyl groups
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/08Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/18Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals

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Abstract

내용 없음

Description

3위치에 치환된 인돌(indole)의 신규의 제조방법 및 본 방법에서 유용한 중간체
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (11)

  1. (a) N-(2-니트로스티릴)엔아민과 알킬화제를 반응시켜 이민염을 수득하는 단계, (b) 상기 이민염과 물을 임의로 반응시켜 (2-니트로페닐)아세트알데히드를 수득하는 단계, 및 (c)상 이민염 또는 (2-니트로페닐)아세트알데히드와 니트로기를 선택적으로 환원시킬 수 있는 환원제를 반응시켜 바람직한 3-알킬화된 인돌을 수득하는 단계를 포함하는 3-알킬화된 인돌의 제조방법.
  2. 제1항에 있어서, 상기 이민염과 물을 반응시켜 (2-니트로페닐)아세트알데히드를 수득하는 방법.
  3. 제1항 또는 제2항에 있어서, 상기 N-(2-니트로스티릴)엔아민이 2-니트로-β-(디-(1-4C)알킬아미노)스티렌, 2-니트로-β-(1-피롤리디닐)스티렌, 2-니트로-β-(1-피페리디닐)-스티렌 또는 2-니트로-β-(4-몰포리닐)스티렌인 것을 특징으로 하는 방법.
  4. 제1항 내지 제3항 중 어느 한항에 있어서, 상기 N-(2-니트로스티릴)엔아민은 하기 일반식(Ⅳ)의 화합물이고, 상기 알킬화제는 하기 일반식 화합물의 방법.
    (상기식에서 각각의 R은 (1-4C)알킬기이거나, 함께 4- 또는 5-원알킬렌이거나 헤테로알킬렌 사슬이고, X는 이탈원자 또는 이탈기이고, T는 COORh, U는 COORj이고, Rh와 Rj는 각각 따로 쉽게 제저할 수 있는 산보호기이다.)
  5. 제1항 내지 제4항 중 어느 한항에 있어서, 상기 환원제가 산의 존재시 철;스태너스 클로라이드;티타늄 트리클로라이드;소듐 니티오나이트;라니 니켈을 갖는 히드라진;또는 전이 금속 수소화 촉매의 존재시 수소인 것을 특징으로 하는 방법.
  6. 제5항에 있어서, 상기 환원제가 아세트산의 존재시 철인 것을 특징으로 하는 방법.
  7. 제1항 내지 제6항중 어느 한항에 있어서, 상기 알킬화 반응과 환원 반응이 0내지 120℃의 온도범위에서 효과적인 것을 특징으로하는 방법.
  8. 제1항 내지 제7항중 어느 한항에 있어서, 상기 이민염을 물과 0내지 100℃에서 반응시키는 방법.
  9. 하기 일반식 Ⅷ의 (2-니트로페닐)아세트알데히드;
    (상기식에서 T는 COORhU는 COORj, 그리고 Rh와 Rj는 각각 따로 페닐, 벤질, 및 아세톡시, (1-4C)알콕시 또는 (1-4C)알킬티오 치환체를 임의로 가지는 (1-6C)알킬중에서 선택된 용이하게 제거할 수 있는 산보호기이다)
  10. 4-[5-(N-[4,4,4-트리플루오르-2-메틸부틸]-카르바모일)-1-메틸인돌-3-일메틸]-3-메톡시-N-O-토릴설포닐-벤자미드의 제조시, 제9항의 (2-니트로페닐)아세트알데히드를 사용하는 방법.
  11. (a)하기 일반식(Ⅴ)의 화합물과 하기 일반식(Ⅳ)의 화합물을 반응시켜 이민염을 수득하는 단계, (b)상기 이민염과 물을 반응시켜 하기 일반식(Ⅷ)의 (2-니트로페닐)아세트알데히드를 수득하는 단계, (c)상기 (2-니트로페닐)아세트 알데히드와 니트로기를 선택적으로 환원시킬 수 있는 환원제를 반응시켜 하기 일반식(Ⅵ)의 화합물을 수득하는 단계, (d) 하기일반식(Ⅵ)의 화합물을 메틸화하여 일반식(Ⅶ)의 화합물을 수득하는 단계, (e)상기 기를 Rh보호기를 제거함으로써, 2-메틸벤젠설폰아al카르보닐기로 전환하고 생성된 카르복실산 또는 그것의 반응 유도체와 2-메틸벤젠설폰아미드 또는 그것의 염을 반응시키는 단계, 및 (f)상기 U기를 Rj보호기를 제거함으로써 2-메틸-4,4,4-트리플루오로 부틸아미노카르보닐기로 전환하고 생성된 카르복실산 또는 그것의 반응 유도체와 2-메틸-4,4,4-트리플루오로부틸아민 또는 그것의 산부가염을 반응시키는 단계를 포함하는 4-[5-(N-[4,4,4-트리플루오로-2-메틸부틸]-카르바모일)-1-메틸인돌-3-일메틸]-3-메톡시-N-O-토릴설포닐벤자미드 제조방법.
    (상기식에서 각각의 R은 따로 (1-4C)알킬이거나, 함께 4-또는 5-원 알킬렌 또는 헤테로알킬렌 사슬이고, X는 이탈원자 또는 이탈기, T는 COORh, U는 COORj, 그리고 Rh및 Rj는 각각 따로 용이하게 제거할 수 있는 산보호기이다.)
    ※ 참고사항 : 최초출원 내용에 의하여 공개되는 것임.
KR1019910022262A 1990-12-05 1991-12-04 (2r)-메틸-4,4,4-트리플루오로부틸아민 또는 이것의 산부가염을 제조하는 방법 KR100228328B1 (ko)

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GB9026427.6 1990-12-05
GB909026427A GB9026427D0 (en) 1990-12-05 1990-12-05 Chemical process
GB9026425.0 1990-12-05

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KR920012029A true KR920012029A (ko) 1992-07-25
KR100228328B1 KR100228328B1 (ko) 1999-11-01

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US (1) US5280125A (ko)
EP (1) EP0489547B1 (ko)
JP (1) JP3160040B2 (ko)
KR (1) KR100228328B1 (ko)
AT (1) ATE168998T1 (ko)
AU (1) AU652002B2 (ko)
CA (1) CA2056065C (ko)
CZ (1) CZ282019B6 (ko)
DE (1) DE69129894T2 (ko)
DK (1) DK0489547T3 (ko)
ES (1) ES2118743T3 (ko)
FI (1) FI102170B1 (ko)
GB (1) GB9026427D0 (ko)
HU (1) HU222123B1 (ko)
IE (1) IE913936A1 (ko)
IL (1) IL100055A (ko)
NO (1) NO175680C (ko)
NZ (1) NZ240624A (ko)
PT (1) PT99683B (ko)
RU (1) RU2054417C1 (ko)
SK (1) SK278987B6 (ko)
ZA (1) ZA919079B (ko)

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GB9119001D0 (en) * 1991-09-05 1991-10-23 Ici Plc Pharmaceutical agents
AU4400597A (en) * 1996-10-08 1998-05-05 Fujisawa Pharmaceutical Co., Ltd. Indole derivatives
CN112457235B (zh) * 2020-12-02 2023-04-25 烟台凯博医药科技有限公司 一种7-甲基吲哚的制备方法

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US3976639A (en) * 1970-11-04 1976-08-24 Hoffmann-La Roche Inc. Intermediates for indoles
US3732245A (en) * 1970-11-04 1973-05-08 Hoffmann La Roche Process and intermediates for the preparation of indoles from ortho-nitrotoluenes
US3979410A (en) * 1974-01-21 1976-09-07 Hoffmann-La Roche Inc. Intermediate α-acyl-β-dialkylamino-2-nitrostyrenes
US4137404A (en) * 1977-12-20 1979-01-30 Hoffmann-La Roche Inc. Synthesis of tryptophans
US4665087A (en) * 1982-02-22 1987-05-12 Ciba-Geigy Corporation 1-(carbamyl, thiocarbamyl, and iminocarbamyl)-indoline derivatives
GB8607294D0 (en) * 1985-04-17 1986-04-30 Ici America Inc Heterocyclic amide derivatives
GB8623429D0 (en) * 1985-10-17 1986-11-05 Ici America Inc Carboximide derivatives
US5180728A (en) * 1989-09-25 1993-01-19 Fujisawa Pharmaceutical Company, Ltd. Pyrimidoindole derivatives and processes for preparation thereof
GB8927981D0 (en) * 1989-12-11 1990-02-14 Ici Plc Carbamoyl derivative
GB9026425D0 (en) * 1990-12-05 1991-01-23 Ici Plc Process

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FI915735A (fi) 1992-06-06
EP0489547B1 (en) 1998-07-29
FI915735A0 (fi) 1991-12-05
CS363391A3 (en) 1992-06-17
KR100228328B1 (ko) 1999-11-01
IL100055A (en) 1996-12-05
NO914775L (no) 1992-06-09
CA2056065A1 (en) 1992-06-06
ZA919079B (en) 1992-09-30
HU913759D0 (en) 1992-02-28
SK278987B6 (sk) 1998-05-06
DE69129894T2 (de) 1998-12-10
PT99683A (pt) 1992-10-30
JP3160040B2 (ja) 2001-04-23
PT99683B (pt) 1999-05-31
AU652002B2 (en) 1994-08-11
NO175680B (no) 1994-08-08
JPH04266870A (ja) 1992-09-22
EP0489547A1 (en) 1992-06-10
FI102170B (fi) 1998-10-30
NO175680C (no) 1994-11-16
ATE168998T1 (de) 1998-08-15
HU222123B1 (hu) 2003-04-28
CA2056065C (en) 2003-07-29
NO914775D0 (no) 1991-12-04
FI102170B1 (fi) 1998-10-30
CZ282019B6 (cs) 1997-04-16
US5280125A (en) 1994-01-18
DE69129894D1 (de) 1998-09-03
DK0489547T3 (da) 1999-04-26
RU2054417C1 (ru) 1996-02-20
AU8794691A (en) 1992-06-11
IE913936A1 (en) 1992-06-17
GB9026427D0 (en) 1991-01-23
HUT60716A (en) 1992-10-28
NZ240624A (en) 1994-01-26
IL100055A0 (en) 1992-08-18
ES2118743T3 (es) 1998-10-01

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