KR850006004A - [(1,3-디 옥소-1,3-프로판디일)디이미노)]비스벤 조산 유도체의 제조방법 - Google Patents
[(1,3-디 옥소-1,3-프로판디일)디이미노)]비스벤 조산 유도체의 제조방법 Download PDFInfo
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- C07D207/33—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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- C07D265/12—1,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems
- C07D265/14—1,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D265/20—1,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring with hetero atoms directly attached in position 4
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- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/54—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
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- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/87—Benzo [c] furans; Hydrogenated benzo [c] furans
- C07D307/88—Benzo [c] furans; Hydrogenated benzo [c] furans with one oxygen atom directly attached in position 1 or 3
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- C—CHEMISTRY; METALLURGY
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- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/32—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings 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
- C07D317/34—Oxygen atoms
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- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/24—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
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Furan Compounds (AREA)
- Pyridine Compounds (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
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- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
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Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
제1 및 2는 각각 실시예 4에서 제조된 결정 a의 IR 스펙트럼 및1H-NMR 스펙트럼을 나타내고
제3도는 각각 실시예 4에서 제조된 결정 c의 스펙트럼 및1H-NMR 스펙트럼을 나타내고
Claims (5)
- 하기의 (a)~(g)의 방법에 의해 하기 일반식(Ⅰ)의 화합물, 및 적용가능한 경우 그의 제약학적으로 허용되는 염을 제조하는 방법:(Ⅰ)상기 식중, A및 B는 둘다 수소이거나 또는 A 및 B중 하나는 일반식(G)의 기이고 다른 하나는 R5기이며, (이때, R1은 임의 치환도니 아릴기 또는 복소환기이고, R4및 R5는 둘다 수소이거나 또는 함께 단일화학 결합을 형성한다.), R2및 R2´는 각각 수소, 할로겐, 니트로, 저급알킬 또는 저급알콕시이고, R3및, R3´는 각각 카로복시 또는 그의 관능유도체이며, 단, (i) A 및 B가 둘다 수소이면 R2및 R2´는 둘다 수소일 수 없고, (ii) A 및 B중 하나가 (G)기 이고 다른하나 R5가(기이때 R4및 R5는 함께 단일화학 결합을 형성)이고, R1은 비치환 아릴이며 R2및 R2´가 둘다 수소이며, R3및, R3´는 각각 카로복시, 또는 메틸에스테를 이외의 그의 관능유도체이다.}, (a)하기 일반식(Ia)의 화합물에서 R3a및 R3a´기를 카르복시기로 전환시켜서 하기 일반식(Ib)의 화합물을 수득하거나,(Ia)(Ib)(상기식중 R3a및 R3a´는 각각 카르복시의 관능 유도체이고, A,B,R2및 R2´는 상기에서 정의한 바와 같다.),(b) 하기 일반식(Ic)의 화합물 또는 그의 금속염을 하기 일반식(Ⅱ)의 화합물 반응시켜서 하기 일반식 (Id)이 화합물을 수득하거나,(Ic)(Id)(상기식중, R1,R2,R2´,R3및 R3´는 상기에서 정의한 바와 같다.),(c)하기일반식(Id)의 화합물을 환원시켜서 하기 일반식(Ie)의 화합물을 수득하거나,(Id)(Ie)(상기식중, R1,R2,R2´,R3및 R3´는 상기에서 정의한 바와 같다.), (d) 하기일반식(Ⅲ)의 하합물 또는 그의 카르록시기의 반응성 유도체를 하기 일반식(Ⅳ)의 화합물 및 하기일반식(Ⅳ´)의 화합물 또는 그들의 아미노기의 반응성 유도체와 반응시켜서 하기일반식(Ⅰ)의 화합물을 수득하거나,(상기식중, A,B,R2,R3,R2´,R3´는 상기에서 정의한 바와 같다.), (e) 하기일반식(Id)의 화합물을 에스테르화 시켜서 하기일반식(If)의 화합물을 수득하거나,(Id)(If)(상기 식중, A,B,R2및 R2´는 상기에서 정의한 바와 같고, R3b 및 R3b´ 는 각각 에스테르화 카르복시이다.), (f) 하기일반식(Ig)의 화합물을 저급알킬화 시켜서 하기 일반식(Ih)의 화합물을 수득하거나,(Ig)(Ih)(상기 식중, R1a는 히드록시로 치환된 아릴이고, R1b는 저급알콕시로 치환된 아릴이며, R2,R2´,R3, R3´,R4및 R5는 상기에서 정의한 바와같다.)또는 (g) 하기 일반식(Ii)의 화합물을 저급알킬화 시켜서 하기 일반식(Ij)의 화합물을 수득한다.(Ii)(Ij)(상기 식중, R1c는 필로릴 또는 인돌릴이고, R1d는 N-저급알킬피롤리딜 또는 N-저급알킬인돌릴이며, R2,R2´,R3, R3´,R4및 R5는 상기에서 정의한 바와 같다.)
- 제1항에 있어서, 방법(e)에서 하기 일반식(Ⅰ)의 화합물 또는 그의 카르복시기의 반응성 유도체를 일반식 R-OH(식중, R은 2개이상의 탄소원자를 갖는 알코올로부터 히드록시기를 제거함으로써 유도되는 잔기이다)의 히드록시 화합물 또는 그의 히드록시기의 반응성 유도체와 반응시켜서 하기 일반식(Ik)의 화합물을 수득함을 특징으로 하는 방법.(Iℓ)(Ik)(상기 식중, R은 상기에서 정의한 바와 같다.)
- (i) 하기 일반식(Il)의 화합물 또는 그의 카르복시기의 반응성 유도체를 메틸화제와 반응시키거나, 또는 (ii) 하기 일반식(In)의 화합물 또는 그의 금속염을 벤즈알데히드와 반응시킴을 특징으로 하는 하기 일반식(Im)의 화합물의 제조방법.(Im)(Iℓ)(In)
- 낮은 녹는점 형테에 마찰력을 가하는 처리를 행함을 특징으로 하는 하기 일반식(Io)의 화합물의 높은 녹는점 형태를 제조하는 방법.(Io)(상기 식중, R´는 페닐, 2-티에닐, 3-티에닐 또는 1-메틸-2-피롤릴이다.)
- (A) 하기 일반식(Ip)의 화합물을 탈수 반응시키거나, 또는 (B) 하기 일반식(Ⅶ)의 화합물을 일반식 R1-CHO(식중, R1은 하기에 정의하는 바와 같다)의 화합물과 반응시킴을 특징으로 하는 하기 일반식(Ⅴ)의 화합물의 제조방법.(상기 식중, R1은 임의 치환된 아릴기 또는 복소환기이고, R2및 R2´는 각각 수소, 할로겐, 니트로, 저급알킬 또는 저급알콕시이다.)※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59022360A JPS60166651A (ja) | 1984-02-08 | 1984-02-08 | 新規ジアミド化合物 |
JP22360/84 | 1984-02-08 |
Publications (1)
Publication Number | Publication Date |
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KR850006004A true KR850006004A (ko) | 1985-09-28 |
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ID=12080462
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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KR1019850000804A KR850006004A (ko) | 1984-02-08 | 1985-02-08 | [(1,3-디 옥소-1,3-프로판디일)디이미노)]비스벤 조산 유도체의 제조방법 |
Country Status (2)
Country | Link |
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JP (1) | JPS60166651A (ko) |
KR (1) | KR850006004A (ko) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5123951A (en) * | 1986-03-31 | 1992-06-23 | Rhone-Poulenc Nederland B.V. | Synergistic plant growth regulator compositions |
WO1987005898A2 (en) * | 1986-03-31 | 1987-10-08 | Rhone-Poulenc Nederlands B.V. | Use of malonic acid derivative compounds for retarding plant growth |
US5877897A (en) | 1993-02-26 | 1999-03-02 | Donnelly Corporation | Automatic rearview mirror, vehicle lighting control and vehicle interior monitoring system using a photosensor array |
US5550677A (en) * | 1993-02-26 | 1996-08-27 | Donnelly Corporation | Automatic rearview mirror system using a photosensor array |
US8017898B2 (en) | 2007-08-17 | 2011-09-13 | Magna Electronics Inc. | Vehicular imaging system in an automatic headlamp control system |
-
1984
- 1984-02-08 JP JP59022360A patent/JPS60166651A/ja active Granted
-
1985
- 1985-02-08 KR KR1019850000804A patent/KR850006004A/ko not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
JPH0422901B2 (ko) | 1992-04-20 |
JPS60166651A (ja) | 1985-08-29 |
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