KR890009904A - 광학적 활성 3-데메틸메발론산 유도체, 및 중간 생성물의 제조방법 - Google Patents
광학적 활성 3-데메틸메발론산 유도체, 및 중간 생성물의 제조방법 Download PDFInfo
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- KR890009904A KR890009904A KR1019880016302A KR880016302A KR890009904A KR 890009904 A KR890009904 A KR 890009904A KR 1019880016302 A KR1019880016302 A KR 1019880016302A KR 880016302 A KR880016302 A KR 880016302A KR 890009904 A KR890009904 A KR 890009904A
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—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
- C07D213/02—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
- 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
- C07D213/54—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
- C07D213/55—Acids; Esters
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/04—1,3-Dioxanes; Hydrogenated 1,3-dioxanes
- C07D319/06—1,3-Dioxanes; Hydrogenated 1,3-dioxanes not condensed with other rings
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Pyrane Compounds (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Pyrrole Compounds (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (3)
1) 일반식(Ⅵ)의 디올 에스테르를 공지방법 자체로 통상적 보호그룹을 도입시켜 일급 알콜 그룹상에서 보호된 일반식(Ⅶ) 화합물로 전환시키고, 2) 일반식(Ⅶ)의 생성 화합물 또는 이의 상응하는 알콜레이트를 t-부틸아세테이트 또는 적절한 등가물로 통상적 축합반응시켜 일반식(Ⅷ) 화합물로 전환시키고, 3) 일반식(Ⅷ)의 생성된 하이드록시 케토에스테르를 공지방법 자체로 일반식(Ⅸ)의 1,3-디올에스테르로 환원시키고, 4) 일반식(Ⅸ)의 생성된 1,3-디올 에스테르를 1,3-디올에 적합한 보호그룹을 도입시켜 일반식(Ⅹ)의 화합물로 전환시키고, 5) 일반식(Ⅹ)의 생성화합물을 통상적 방법으로 보호그룹 R2를 제거하여 일반식(Ⅲ)의 화합물로 전환시키고, 6) 일반식(Ⅲ)의 생성 화합물을 일반식(XI)의 올레핀 유도체로 전환시키고, 7) 일반식(XI)의 생성화합물을 가수분해시켜 Y가 CH=CH 그룹으로, R1이 C1-C8-알킬 라디칼인 일반식(Ⅰ)의 화합물을 수득하고, 8) 경우에 따라 Y가 CH=CH 그룹인 일반식(Ⅰ)의 생성 화합물을 수소화반응시켜 Y가 CH2-CH2그룹인 일반식(Ⅰ) 화합물을 수득하고, 9) 경우에 따라 생성 화합물을 산(R1=H) 또는 염(R1=금속 양이온)으로 전환시키고, 10) 경우에 따라 일반식(Ⅰ)의 생성 화합물을 일반식(Ⅱ)의 화합물로 전환시킴을 특징으로 하여, 일반식(Ⅰ) 또는 일반식(Ⅱ)의 광학적 활성 3-데메틸 메발론산 유도체를 제고하는 방법.
상기식에서, Y는 -CH=CH- 또는 -CH2-CH2-그룹이고, R은 일반식(α) 또는 (β)의 라디칼이고,
Z는 구조식 -CH의 라디칼이거나 질소원자이고, R3,R4및 R5는 서로 독립적으로, 수소, 탄소수 3 내지 6의 포화 또는 불포화 환식 탄화수소 라디칼에 의해 말단 탄소에서 임의로 치환될 수 있는 탄소수 6이하의 직쇄 또는 측쇄 탄화수소 라디칼이거나, 탄소수 3 내지 7 이하의 환식 포화되거나 이중으로 불포화된 탄화수소 라디칼, 할로겐, 트리플루오로메틸, 각각의 경우 탄소수 6이하의 알킬 또는 알케닐, 하이드록실, 탄소수 1 내지 6의 알콕시, 카복실, 또는 알콕시 잔기중의 탄소수가 1 내지 6인 카브알콕시중에서 선택된 동일하거나 상이한 1 내지 3개의 치환체들을 핵중에 임의로 함유할 수 있는 페닐, 푸릴, 티에닐 및 피리딜중에서 선택된 방향족 라디칼이고, A-B는 -CH-CH- 또는 -C=C- 그룹이고, R6및 R7는 동일하거나 상이하고, 탄소수 1 내지 6의 알콕시 그룹 또는 그룹(여기에서, R9은 탄소수 1 내지 8의 알킬이다)에 의해 치환될 수 있는 탄소수 20이하의 포화되거나 불포화된 알킬 라디칼이거나, 방향족 라디칼이 할로겐, 각각의 경우 탄소수 1 내지 6의 알킬 또는 알콕시, 탄소수 3 내지 7의 사이클로알킬 또는 그룹(여기에서, R9는 탄소수 1 내지 8의 알킬이다)에 의해 핵중에서 1 내지 3회 치환될 수 있는 탄소수 3 내지 7의 사이클로알킬 라디칼, 페닐, 티에닐, 푸릴 또는 나프틸 라디칼, 또는 탄소수 1 내지 4의 알킬에 의해 핵중에서 1 내지 3회 치환될 수 있는 피리딜 라디칼이고, R8은 탄소수 8이하의 포화되거나 불포화된 알킬 라디칼, 할로겐, 각각의 경우 탄소수 1 내지 4의 알콕시 또는 알킬에 의해 핵중에서 1 내지 3회 치환될 수 있는 벤질 라디칼, 페닐, 티에틸, 푸릴 또는 나프틸 라디칼(여기에서, 방향족 라디칼을 각각의 경우 할로겐, 탄소수 1 내지 4의 알콕시 또는 알킬 또는 탄소수 3 내지 7의 사이클로알킬 라디칼에 의해 핵중에서 1 내지 3회 치환될 수 있다)이며, R1은 수소, 금속 양이온 또는 탄소수 1 내지 8의 알킬 라디칼이고, 일반식(Ⅵ),(Ⅶ),(Ⅷ),(Ⅸ),(Ⅹ),(Ⅲ) 및 (Ⅵ)에서, R1은 C1-C8-알킬이고, R2는 통상의 알콜 보호그룹이며, M은 1,3-디올류에 대한 적절한 보호그룹이다.
일반식(XII)의 알데히드.
상기식에서, M은 하기 구조식
의 라디칼이다.
M이 일반식(XII)에서 나타낸 정의를 갖는 일반식(Ⅲ)의 알콜을 산화시킴을 특징으로하여, 일반식(XII)의 알데히드를 제조하는 방법.
※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEP3741509.3 | 1987-12-08 | ||
DE19873741509 DE3741509A1 (de) | 1987-12-08 | 1987-12-08 | Verfahren zur herstellung optisch aktiver 3-desmethylmevalonsaeurederivate sowie zwischenprodukte |
Publications (2)
Publication Number | Publication Date |
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KR890009904A true KR890009904A (ko) | 1989-08-04 |
KR970008314B1 KR970008314B1 (ko) | 1997-05-23 |
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Application Number | Title | Priority Date | Filing Date |
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KR1019880016302A KR970008314B1 (ko) | 1987-12-08 | 1988-12-08 | 광학적 활성 3-데메틸메발론산 유도체 및 중간 생성물의 제조방법 |
Country Status (18)
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US (2) | US4970313A (ko) |
EP (1) | EP0319847B1 (ko) |
JP (2) | JP2511510B2 (ko) |
KR (1) | KR970008314B1 (ko) |
AT (1) | ATE92045T1 (ko) |
AU (2) | AU616224B2 (ko) |
CA (1) | CA1340105C (ko) |
DE (2) | DE3741509A1 (ko) |
DK (1) | DK170616B1 (ko) |
ES (1) | ES2058222T3 (ko) |
FI (1) | FI92321C (ko) |
HU (2) | HU207045B (ko) |
IE (1) | IE62540B1 (ko) |
IL (1) | IL88612A (ko) |
NO (1) | NO174201C (ko) |
NZ (1) | NZ227210A (ko) |
PT (1) | PT89163B (ko) |
ZA (1) | ZA889120B (ko) |
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CN104230879B (zh) * | 2014-08-15 | 2016-08-24 | 新发药业有限公司 | 一种2-((4r, 6s)-6-甲酰基-2,2-二取代基-1,3-二氧六环-4-基)乙酸酯制备方法 |
CN105985311B (zh) * | 2015-02-15 | 2019-08-13 | 北大医药股份有限公司 | 一种制备瑞舒伐他汀钙的中间体及其制备瑞舒伐他汀钙的方法 |
CN106317011B (zh) * | 2015-06-25 | 2019-01-18 | 北大方正集团有限公司 | 一种瑞舒伐他汀钙中间体的制备方法 |
CN115894431A (zh) * | 2022-11-29 | 2023-04-04 | 南京欧信医药技术有限公司 | 他汀类药物中间体的制备方法 |
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US4571428A (en) * | 1983-07-08 | 1986-02-18 | Sandoz, Inc. | 6-Substituted-4-hydroxy-tetrahydropyran-2-ones |
EP0244364A3 (en) * | 1986-04-30 | 1992-04-01 | Sandoz Ag | Preparation of olefinic compounds |
US4681893A (en) * | 1986-05-30 | 1987-07-21 | Warner-Lambert Company | Trans-6-[2-(3- or 4-carboxamido-substituted pyrrol-1-yl)alkyl]-4-hydroxypyran-2-one inhibitors of cholesterol synthesis |
US4897490A (en) * | 1987-02-25 | 1990-01-30 | Bristol-Meyers Company | Antihypercholesterolemic tetrazole compounds |
EP0307342B1 (de) * | 1987-07-10 | 1996-01-03 | Hoechst Aktiengesellschaft | 3-Desmethyl-mevalonsäurederivate, Verfahren zu ihrer Herstellung, pharmazeutische Präparate auf Basis dieser Verbindungen, ihre Verwendung sowie Zwischenprodukte |
US4906624A (en) * | 1987-09-08 | 1990-03-06 | Warner-Lambert Company | 6-(((Substituted)pyridin-3-yl)alkyl)-and alkenyl)-tetrahydro-4-hydroxypyran-2-one inhibitors of cholesterol biosynthesis |
US4824959A (en) * | 1988-02-18 | 1989-04-25 | Bristol-Myers Company | Intermediates for antihypercholesterolemic tetrazole compounds |
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KR20160040875A (ko) * | 2014-10-06 | 2016-04-15 | 한양대학교 에리카산학협력단 | 다이플루오로알킬기가 도입된 유기 화합물의 제조 방법 |
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