KR830010039A - 페닐 지방성 카복실린산 유도체의 제조방법 - Google Patents
페닐 지방성 카복실린산 유도체의 제조방법 Download PDFInfo
- Publication number
- KR830010039A KR830010039A KR1019820001678A KR820001678A KR830010039A KR 830010039 A KR830010039 A KR 830010039A KR 1019820001678 A KR1019820001678 A KR 1019820001678A KR 820001678 A KR820001678 A KR 820001678A KR 830010039 A KR830010039 A KR 830010039A
- Authority
- KR
- South Korea
- Prior art keywords
- formula
- product
- hydrogen atom
- necessary
- iii
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 title 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 title 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 5
- 239000002253 acid Substances 0.000 claims 2
- -1 amine salts Chemical class 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 125000005809 3,4,5-trimethoxyphenyl group Chemical group [H]C1=C(OC([H])([H])[H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 claims 1
- 239000003513 alkali Substances 0.000 claims 1
- 125000005907 alkyl ester group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 239000012024 dehydrating agents Substances 0.000 claims 1
- 230000032050 esterification Effects 0.000 claims 1
- 238000005886 esterification reaction Methods 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 239000007858 starting material Substances 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/02—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
- C07D295/027—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/76—Unsaturated compounds containing keto groups
- C07C59/90—Unsaturated compounds containing keto groups containing singly bound oxygen-containing groups
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (4)
- 다음 구조식(Ⅱ)의 글리옥실린산 또는 하나의 그 알킬에스테르를 다음 구조식(Ⅲ)의 아세톤페논과 반응시켜 A가 수소원자를 나타내고 B가 히드록시 그룹을 나타내는 구조식(Ⅰ)의 생성물에 상응하는 구조식(ⅠA)의 생성물을 얻고, 또는 A및 B가 다같이 (E)배위의 이중 결합을 나타내는 구조식(Ⅰ)의 생성물에 상응하는구조식(ⅠB)의 생성물을 얻고, 필요하다면 구조식(ⅠA)의 생성물을 탈수제에 주입시켜 (E)배위의 구조식(ⅠB)에 상응하는 생성물을 얻고, 그리고 필요하다면 구조식(ⅠA)의 얻어진 생성물을 그것의 광학활성 이성체로 회절시키고, 그리고 필요하다면 (E)배위의 구조식(ⅠB)의 화합물을 이성화시켜 (Z)배위의 구조식(ⅠB)의 화합물을 형성시키고 그리고 필요하다면 R이 수소 원자를 나타내는 구조식(Ⅰ)의 얻어진 생성물을 통상적인 방법에 따라 염기화 또는 에스테르화시킴을 특징으로 하는 가능한 다른 입체 이성질체로 다음 구조식(Ⅰ)의 생성물들뿐 아니라 R이 수소원자를 나타내는 구조식(Ⅰ)의 생성물의 알칼리, 알칼리-도 또는 아민 염들의 제조방법.(Ⅰ)OHC-COOR (Ⅱ)(Ⅲ)상기 구조식에서세개의 메톡시 기들은 3,4,5 또는 2,4,6 또는 2,3,5 또는 2,3,6위에 위치하고 여기서 A 및 B는 다같이 이중결합을 나타내거나 A는 수소 원자를 나타내고 B는 히드록 시기를 나타내고 R은 수소 원자 또는 1내지 5탄소 함유의 알킬기를 나타낸다.
- 1항에 있어서 세개의 메톡시 기들이 3,4,5 또는 2,4,5위에 위치하는 구조식(Ⅲ)의 아세톤페논을 출발물질로 사용함을 특징으로 하는 1항에 따른 제조방법.
- (E) 4-(3,4,5-트리메톡시페닐) 4-옥소 2-부레노인산이 제조됨을 특징으로 하는 1 또는 2항에 따른 제조방법.
- (E) 4-(2,4,5-트리메톡시페닐) 4-옥소 2-부테노인산이 제조됨을 특징으로 하는 1항 또는 2항에 따른 제조방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR81-07801 | 1981-04-17 | ||
FR8107801A FR2504127B1 (fr) | 1981-04-17 | 1981-04-17 | Nouveaux derives d'acides phenyl aliphatique carboxyliques, procede pour leur preparation et leur application comme medicaments |
Publications (2)
Publication Number | Publication Date |
---|---|
KR830010039A true KR830010039A (ko) | 1983-12-24 |
KR870001537B1 KR870001537B1 (ko) | 1987-09-02 |
Family
ID=9257553
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR8201678A KR870001537B1 (ko) | 1981-04-17 | 1982-04-16 | 페닐지방성 카복실린산유도체의 제조방법 |
Country Status (27)
Country | Link |
---|---|
US (1) | US4450292A (ko) |
JP (2) | JPS57183736A (ko) |
KR (1) | KR870001537B1 (ko) |
AT (1) | AT390054B (ko) |
AU (1) | AU550822B2 (ko) |
BE (1) | BE892886A (ko) |
CA (1) | CA1168255A (ko) |
CH (1) | CH652387A5 (ko) |
DE (1) | DE3214082A1 (ko) |
DK (1) | DK157673C (ko) |
ES (1) | ES8303279A1 (ko) |
FI (1) | FI73965C (ko) |
FR (1) | FR2504127B1 (ko) |
GB (1) | GB2096999B (ko) |
GR (1) | GR75457B (ko) |
HU (1) | HU186857B (ko) |
IE (1) | IE52444B1 (ko) |
IL (1) | IL65445A (ko) |
IT (1) | IT1147846B (ko) |
LU (1) | LU84090A1 (ko) |
MA (1) | MA19444A1 (ko) |
NL (1) | NL8201579A (ko) |
OA (1) | OA07539A (ko) |
PT (1) | PT74767B (ko) |
SE (1) | SE453493B (ko) |
SU (1) | SU1264836A3 (ko) |
ZA (1) | ZA822571B (ko) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2515037A1 (fr) * | 1981-10-22 | 1983-04-29 | Roussel Uclaf | A titre de medicaments, certains derives mono-substitues de l'acide 4-phenyl 4-oxo buten-2-oique, ainsi que les compositions les renfermant |
IT1190340B (it) * | 1986-06-06 | 1988-02-16 | Roussel Maestretti Spa | Derivati dell'acido 4-fenil 4-osso 2-butenoico,loro procedimento di preparazione e loro impiego come prodotti medicinali |
DK49688A (da) * | 1987-03-20 | 1988-09-21 | Hoffmann La Roche | Propiolophenonderivater |
HU198294B (en) * | 1987-06-10 | 1989-09-28 | Richter Gedeon Vegyeszet | Process for producing butenoic acid amides and pharmaceutical compositions comprising such active ingredient |
US4777288A (en) * | 1987-06-11 | 1988-10-11 | Pfizer Inc. | Process for preparing a 4,4-diphenylbutanoic acid derivative |
DE3881770T2 (de) * | 1987-07-20 | 1993-10-07 | Cometec Srl | Zusammensetzungen zum Fördern der Tierwachstums. |
HU198446B (en) * | 1987-09-25 | 1989-10-30 | Richter Gedeon Vegyeszet | Process for production of new amids of buten acid and medical compositions containing such active substances |
US5849729A (en) * | 1995-12-26 | 1998-12-15 | Hershey Foods Corporation | Use of hydrolyzed cocoa butter for percutaneous absorption |
US5837227A (en) * | 1995-12-26 | 1998-11-17 | Hershey Foods Corporation | Use of cocoa butter or partially hydrolyzed cocoa butter for the treatment of burns and wounds |
GB9816358D0 (en) | 1998-07-27 | 1998-09-23 | Angeletti P Ist Richerche Bio | Enzyme inhibitors |
JP2003525200A (ja) | 1998-07-27 | 2003-08-26 | イスティトゥト ディ リチェルケ ディ ビオロジア モレコラーレ ピー.アンジェレッティ ソチエタ ペル アツィオニ | ポリメラーゼ阻害剤としてのジケト酸誘導体 |
RU2771565C1 (ru) * | 2021-05-28 | 2022-05-05 | Общество С Ограниченной Ответственностью "Валента-Интеллект" | Новые соединения |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE708617A (ko) * | 1966-12-30 | 1968-06-28 | ||
NL6717403A (ko) * | 1966-12-30 | 1968-07-01 | ||
US3857949A (en) * | 1970-06-26 | 1974-12-31 | Inst Chemioterapico Italiano S | Prophylaxis and treatment of cardiac disorders |
US3803222A (en) * | 1970-06-26 | 1974-04-09 | Istituto Chem It Spa | Oxo-trialkoxyphenyl-alkanoic acids and salts thereof |
DE2116293A1 (de) * | 1971-04-02 | 1972-10-19 | Cassella Farbwerke Mainkur Ag, 6000 Frankfurt | Ketonderivate und Verfahren zu ihrer Herstellung |
BE788749A (fr) * | 1971-09-13 | 1973-03-13 | Takeda Chemical Industries Ltd | Acide 3-(benzoyl trisubstitue)-propionique et son procede de preparation |
US4017517A (en) * | 1971-09-13 | 1977-04-12 | Takeda Chemical Industries, Ltd. | 2-(Trisubstituted benzoyl)-propionic acid and a method for the production thereof |
AT319215B (de) * | 1972-09-13 | 1974-12-10 | Takeda Chemical Industries Ltd | Verfahren zur Herstellung von neuen 3-(2',4',5'-trisubst. Benzoyl)-propionsäuren |
FR2481118A1 (fr) * | 1980-04-24 | 1981-10-30 | Roussel Uclaf | Application a titre de medicaments de derives substitues de l'acide phenyl-4-oxo-2-butenoique |
-
1981
- 1981-04-17 FR FR8107801A patent/FR2504127B1/fr not_active Expired
-
1982
- 1982-03-23 SE SE8201840A patent/SE453493B/sv not_active IP Right Cessation
- 1982-04-06 IL IL65445A patent/IL65445A/xx unknown
- 1982-04-12 GR GR67892A patent/GR75457B/el unknown
- 1982-04-13 MA MA19649A patent/MA19444A1/fr unknown
- 1982-04-14 AT AT0144682A patent/AT390054B/de not_active IP Right Cessation
- 1982-04-14 FI FI821305A patent/FI73965C/fi not_active IP Right Cessation
- 1982-04-14 US US06/368,208 patent/US4450292A/en not_active Expired - Fee Related
- 1982-04-15 ZA ZA822571A patent/ZA822571B/xx unknown
- 1982-04-15 NL NL8201579A patent/NL8201579A/nl not_active Application Discontinuation
- 1982-04-16 IT IT48240/82A patent/IT1147846B/it active
- 1982-04-16 DE DE19823214082 patent/DE3214082A1/de not_active Ceased
- 1982-04-16 PT PT74767A patent/PT74767B/pt unknown
- 1982-04-16 JP JP57062641A patent/JPS57183736A/ja active Granted
- 1982-04-16 KR KR8201678A patent/KR870001537B1/ko active
- 1982-04-16 AU AU82690/82A patent/AU550822B2/en not_active Ceased
- 1982-04-16 BE BE0/207859A patent/BE892886A/fr not_active IP Right Cessation
- 1982-04-16 IE IE896/82A patent/IE52444B1/en unknown
- 1982-04-16 DK DK170382A patent/DK157673C/da active IP Right Grant
- 1982-04-16 SU SU823423751A patent/SU1264836A3/ru active
- 1982-04-16 CA CA000401128A patent/CA1168255A/fr not_active Expired
- 1982-04-16 ES ES511489A patent/ES8303279A1/es not_active Expired
- 1982-04-16 CH CH2342/82A patent/CH652387A5/fr not_active IP Right Cessation
- 1982-04-16 LU LU84090A patent/LU84090A1/fr unknown
- 1982-04-16 HU HU821177A patent/HU186857B/hu not_active IP Right Cessation
- 1982-04-19 GB GB8211278A patent/GB2096999B/en not_active Expired
-
1983
- 1983-09-22 OA OA58109A patent/OA07539A/xx unknown
-
1987
- 1987-01-26 JP JP62014322A patent/JPS62174012A/ja active Granted
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