NZ206919A - Analogues of mevalonolactone, derivatives thereof and pharmaceutical compositions - Google Patents
Analogues of mevalonolactone, derivatives thereof and pharmaceutical compositionsInfo
- Publication number
- NZ206919A NZ206919A NZ206919A NZ20691984A NZ206919A NZ 206919 A NZ206919 A NZ 206919A NZ 206919 A NZ206919 A NZ 206919A NZ 20691984 A NZ20691984 A NZ 20691984A NZ 206919 A NZ206919 A NZ 206919A
- Authority
- NZ
- New Zealand
- Prior art keywords
- hydrogen
- group
- methyl
- ethyl
- compound
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
- C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
- C07C29/14—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of a —CHO group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C31/34—Halogenated alcohols
- C07C31/38—Halogenated alcohols containing only fluorine as halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/202—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring the aromatic ring being a naphthalene
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/225—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
- C07C45/511—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups
- C07C45/513—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups the singly bound functional group being an etherified hydroxyl group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/56—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/20—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
- C07C47/24—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/52—Compounds having —CHO groups bound to carbon atoms of six—membered aromatic rings
- C07C47/575—Compounds having —CHO groups bound to carbon atoms of six—membered aromatic rings containing ether groups, groups, groups, or groups
-
- 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
- C07C59/42—Unsaturated compounds containing hydroxy or O-metal groups
- C07C59/56—Unsaturated compounds containing hydroxy or O-metal groups containing halogen
-
- 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
- C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups
- C07C59/64—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/732—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids of unsaturated hydroxy carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D263/10—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D263/12—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with radicals containing only hydrogen and carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/16—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D309/28—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
- C07D309/30—Oxygen atoms, e.g. delta-lactones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pyrane Compounds (AREA)
- Confectionery (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicinal Preparation (AREA)
- Furan Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US46060083A | 1983-01-24 | 1983-01-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NZ206919A true NZ206919A (en) | 1987-08-31 |
Family
ID=23829363
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NZ206919A NZ206919A (en) | 1983-01-24 | 1984-01-24 | Analogues of mevalonolactone, derivatives thereof and pharmaceutical compositions |
Country Status (19)
| Country | Link |
|---|---|
| EP (1) | EP0117228B1 (enExample) |
| JP (1) | JPS60500499A (enExample) |
| KR (1) | KR840007555A (enExample) |
| AT (1) | ATE23326T1 (enExample) |
| AU (1) | AU570942B2 (enExample) |
| CA (1) | CA1268473A (enExample) |
| DE (1) | DE3461180D1 (enExample) |
| DK (1) | DK454184A (enExample) |
| ES (1) | ES8609193A1 (enExample) |
| FI (1) | FI843560L (enExample) |
| GR (1) | GR81711B (enExample) |
| HU (1) | HU199769B (enExample) |
| IE (1) | IE840153L (enExample) |
| IL (1) | IL70767A (enExample) |
| NZ (1) | NZ206919A (enExample) |
| PL (1) | PL144594B1 (enExample) |
| PT (1) | PT77996B (enExample) |
| WO (1) | WO1984002903A1 (enExample) |
| ZA (1) | ZA84547B (enExample) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4613610A (en) * | 1984-06-22 | 1986-09-23 | Sandoz Pharmaceuticals Corp. | Cholesterol biosynthesis inhibiting pyrazole analogs of mevalonolactone and its derivatives |
| US5001255A (en) * | 1984-12-04 | 1991-03-19 | Sandoz Pharm. Corp. | Idene analogs of mevalonolactone and derivatives thereof |
| ATE60571T1 (de) * | 1984-12-04 | 1991-02-15 | Sandoz Ag | Inden-analoga von mevalonolakton und ihre derivate. |
| US4668794A (en) * | 1985-05-22 | 1987-05-26 | Sandoz Pharm. Corp. | Intermediate imidazole acrolein analogs |
| US4851427A (en) * | 1985-10-25 | 1989-07-25 | Sandoz Pharm. Corp. | Pyrrole analogs of mevalonolactone, derivatives thereof and pharmaceutical use |
| KR900001212B1 (ko) * | 1985-10-25 | 1990-02-28 | 산도즈 파마슈티칼스 코오포레이숀 | 메바로노락톤 및 그것의 유도체의 헤테로사이클릭 유사체 및 그것의 생산방법 및 약학적인 그것의 용도 |
| ZW10287A1 (en) * | 1986-07-15 | 1988-01-13 | Hoffmann La Roche | Tetrahydronaphthaline and indane derivatives |
| US4751235A (en) * | 1986-12-23 | 1988-06-14 | Sandoz Pharm. Corp. | Anti-atherosclerotic indolizine derivatives |
| IL83821A0 (en) * | 1986-09-10 | 1988-02-29 | Sandoz Ag | Azaindole and indolizine derivatives,their production and pharmaceutical compositions containing them |
| US4898949A (en) * | 1987-02-25 | 1990-02-06 | Bristol-Myers Company | Intermediates for the preparation of antihypercholesterolemic tetrazole compounds |
| US4897490A (en) * | 1987-02-25 | 1990-01-30 | Bristol-Meyers Company | Antihypercholesterolemic tetrazole compounds |
| US5091378A (en) * | 1987-05-22 | 1992-02-25 | E. R. Squibb & Sons, Inc. | Phosphorus-containing HMG-CoA reductase inhibitors, new intermediates and method |
| US4904646A (en) * | 1987-05-22 | 1990-02-27 | E. R. Squibb & Sons, Inc. | Phosphorus-containing HMG-COA reductase inhibitors |
| US5010205A (en) * | 1988-08-23 | 1991-04-23 | Bristol-Myers Company | Antihypercholesterolemic tetrazol-1-yl intermediates |
| US5506219A (en) * | 1988-08-29 | 1996-04-09 | E. R. Squibb & Sons, Inc. | Pyridine anchors for HMG-CoA reductase inhibitors |
| WO2006123355A2 (en) * | 2004-11-03 | 2006-11-23 | Sun Pharmaceutical Industries Limited | Novel statin derivatives |
| WO2013015340A1 (ja) * | 2011-07-25 | 2013-01-31 | 東ソー株式会社 | 2-ハロゲン化アリール-1-ナフタルアルデヒド化合物、その製造法、および、該化合物からトリアリールアミン化合物を製造する方法 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5559140A (en) * | 1978-10-30 | 1980-05-02 | Sankyo Co Ltd | 3,5-dihydroxypentanoic alkyl ester derivative, its preparation and remedy for hyperlipemia containing the same as the effective component |
| AU548996B2 (en) * | 1980-02-04 | 1986-01-09 | Merck & Co., Inc. | Tetrahydro-2h-pyran-2-one derivatives |
-
1984
- 1984-01-23 DE DE8484810039T patent/DE3461180D1/de not_active Expired
- 1984-01-23 PT PT77996A patent/PT77996B/pt not_active IP Right Cessation
- 1984-01-23 AT AT84810039T patent/ATE23326T1/de not_active IP Right Cessation
- 1984-01-23 ES ES529090A patent/ES8609193A1/es not_active Expired
- 1984-01-23 CA CA000445903A patent/CA1268473A/en not_active Expired - Lifetime
- 1984-01-23 EP EP84810039A patent/EP0117228B1/en not_active Expired
- 1984-01-23 IE IE840153A patent/IE840153L/xx unknown
- 1984-01-23 GR GR73574A patent/GR81711B/el unknown
- 1984-01-24 IL IL70767A patent/IL70767A/xx unknown
- 1984-01-24 ZA ZA84547A patent/ZA84547B/xx unknown
- 1984-01-24 WO PCT/EP1984/000018 patent/WO1984002903A1/de not_active Ceased
- 1984-01-24 KR KR1019840000290A patent/KR840007555A/ko not_active Ceased
- 1984-01-24 PL PL1984245886A patent/PL144594B1/pl unknown
- 1984-01-24 NZ NZ206919A patent/NZ206919A/en unknown
- 1984-01-24 FI FI843560A patent/FI843560L/fi not_active Application Discontinuation
- 1984-01-24 AU AU24331/84A patent/AU570942B2/en not_active Ceased
- 1984-01-24 HU HU84660A patent/HU199769B/hu not_active IP Right Cessation
- 1984-01-24 JP JP59500672A patent/JPS60500499A/ja active Pending
- 1984-09-21 DK DK454184A patent/DK454184A/da not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| GR81711B (enExample) | 1984-12-12 |
| KR840007555A (ko) | 1984-12-08 |
| FI843560A7 (fi) | 1984-09-11 |
| PT77996A (en) | 1984-02-01 |
| DK454184D0 (da) | 1984-09-21 |
| IE840153L (en) | 1984-07-24 |
| HU199769B (en) | 1990-03-28 |
| AU2433184A (en) | 1984-08-15 |
| WO1984002903A1 (fr) | 1984-08-02 |
| DK454184A (da) | 1984-09-21 |
| DE3461180D1 (en) | 1986-12-11 |
| IL70767A (en) | 1988-06-30 |
| ATE23326T1 (de) | 1986-11-15 |
| ES8609193A1 (es) | 1986-07-16 |
| FI843560A0 (fi) | 1984-09-11 |
| EP0117228B1 (en) | 1986-11-05 |
| FI843560L (fi) | 1984-09-11 |
| AU570942B2 (en) | 1988-03-31 |
| HUT37380A (en) | 1985-12-28 |
| PL245886A1 (en) | 1985-12-03 |
| IL70767A0 (en) | 1984-04-30 |
| ES529090A0 (es) | 1986-07-16 |
| EP0117228A1 (en) | 1984-08-29 |
| JPS60500499A (ja) | 1985-04-11 |
| ZA84547B (en) | 1985-09-25 |
| PL144594B1 (en) | 1988-06-30 |
| PT77996B (en) | 1986-05-30 |
| CA1268473A (en) | 1990-05-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA1210405A (en) | Analogs of mevalolactone and derivatives thereof | |
| NZ206919A (en) | Analogues of mevalonolactone, derivatives thereof and pharmaceutical compositions | |
| US4668794A (en) | Intermediate imidazole acrolein analogs | |
| US4739073A (en) | Intermediates in the synthesis of indole analogs of mevalonolactone and derivatives thereof | |
| US5354772A (en) | Indole analogs of mevalonolactone and derivatives thereof | |
| US5043330A (en) | Phenol substituted gem-diphosphonate derivatives, process for their preparation and pharmaceutical compositions containing them | |
| US4940800A (en) | Beazimidazole compounds active as inhibitors of the cholesterol biosynthesis | |
| US4474971A (en) | (Tetrahydropyran-2-yl)-aldehydes | |
| EP0244364A2 (en) | Preparation of olefinic compounds | |
| KR900009006B1 (ko) | 메발로락톤의 동족체 및 그것의 유도체의 제조방법 | |
| McGowan et al. | Total synthesis of racemic chorismic acid and (-)-5-enolpyruvylshikimic acid (" compound Z1") | |
| US4808607A (en) | Imidazole analogs of mevalonolactone and derivatives thereof for use in inhibiting cholesterol biosynthesis and lowering blood cholesterol level | |
| US4939159A (en) | Azaindole derivatives useful as cholesterol biosynthesis inhibitors | |
| IE60518B1 (en) | Process for the preparation of (+)-biotin | |
| US5545758A (en) | Process for the preparation of diisopinocampheylchloroborane | |
| EP0299484B1 (en) | Process for the preparation of intermediates for the synthesis of fosfomycin | |
| EP0060416A1 (en) | New beta-lactam acetic acid derivatives, the process for preparing them, and their use as intermediates for 1-azabicyclo(3.2.0.)hept-2-ene antibiotics | |
| JP2714018B2 (ja) | 新規不飽和アミノ酸類の製造方法 | |
| US4755606A (en) | Imidazolyl-3,5-di-(diphenyl-butylsilyloxy) carboxylic acid ester intermediates | |
| Kozikowski et al. | Synthesis and biological activity of the D-3-deoxy-3-fluoro and D-3-chloro-3-deoxy analogs of phosphatidylinositol | |
| Ponpipom et al. | Synthesis of azide and amide analogs of platelet-activating factor and related derivatives | |
| US5091549A (en) | Synthesis of d-myoinositol-1-phosphate | |
| JPH02282388A (ja) | 1,3―置換テトラヒドロ―1H―チエノ―〔3,4―d〕―イミダゾール―2(3H)―オン―4―イリデン―ペンタン酸エステルの製造方法 | |
| CS204595B1 (en) | Process for preparirng analogs of prostaglandin f2alpha | |
| JPH0770053A (ja) | フッ素化ビタミンd誘導体および製造方法 |