ES8106152A1 - Un procedimiento para la preparacion de derivados de 4-hidroxi-tetrahidropiran 2- ona. - Google Patents
Un procedimiento para la preparacion de derivados de 4-hidroxi-tetrahidropiran 2- ona.Info
- Publication number
- ES8106152A1 ES8106152A1 ES494301A ES494301A ES8106152A1 ES 8106152 A1 ES8106152 A1 ES 8106152A1 ES 494301 A ES494301 A ES 494301A ES 494301 A ES494301 A ES 494301A ES 8106152 A1 ES8106152 A1 ES 8106152A1
- Authority
- ES
- Spain
- Prior art keywords
- dihydroxy acids
- phenylethenyl
- ones
- preparing
- stereoisomeric forms
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
- C07C67/343—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C67/347—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by addition to unsaturated carbon-to-carbon bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Communicable Diseases (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Pyrane Compounds (AREA)
- Steroid Compounds (AREA)
- Saccharide Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
PROCEDIMIENTO PARA LA PREPARACION DE DERIVADOS DE 4-HIDROXITETRAHIDROPIRAN 2-ONA. SE REFIERE A LA PREPARACION DE COMPUESTOS DE ESTRUCTURA (I), DONDE A ES HIDROGENO O METILO, E ES UN ENLACE DEL TIPO (II) O (III), R1 ESTA SITUADO EN POSICION ORTO RESPECTO AL RADICAL E Y ES HALOFENILOXI, HALOFENIALCOXI O HALOFENILO, ESPECIALMENTE DONDE HALO ES FLUOR O CLORO; R2 Y R3 SON HALO, ESPECIALMENTE CLORO, EN LAS POSICIONES 4 Y 6. TAMBIEN SE REFIERE A LOS HIDROXIACIDOS RESULTANTES DE LA APERTURA HIDROLITICA DEL ANILLO DE LACTONA, LAS SALES FARMACEUTICAMENTE ACEPTABLES DE LOS HIDROXIACIDOS Y LOS ESTERES ALQUILICOS INFERIORES, FENILICOS Y DIMETILAMINO. PARA SU PREPARACION SE HACE REACCIONAR EL DIANION DE UN ESTER ACETOACETICO CON UN ALDEHIDO DE ESTRUCTURA (IV). SE REDUCE EL GRUPO 3-CETO A GRUPO HIDROXILO. SE SAPONIFICA EL ESTER Y SE LACTONIZA EL CARBOXILO CON EL 6-HIDROXILO. SE UTILIZAN COMO INHIBIDORES DE LA SINTESIS DEL COLESTEROL. *FORMULA*
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US6757479A | 1979-08-17 | 1979-08-17 |
Publications (2)
Publication Number | Publication Date |
---|---|
ES8106152A1 true ES8106152A1 (es) | 1981-07-16 |
ES494301A0 ES494301A0 (es) | 1981-07-16 |
Family
ID=22076933
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES494301A Granted ES494301A0 (es) | 1979-08-17 | 1980-08-14 | Un procedimiento para la preparacion de derivados de 4-hidroxi-tetrahidropiran 2- ona. |
Country Status (24)
Country | Link |
---|---|
EP (1) | EP0024348B1 (es) |
JP (1) | JPS5645470A (es) |
KR (1) | KR840002170B1 (es) |
AT (1) | ATE16487T1 (es) |
AU (1) | AU6108580A (es) |
CA (1) | CA1137989A (es) |
CS (1) | CS219921B2 (es) |
DD (1) | DD152558A5 (es) |
DE (1) | DE3071230D1 (es) |
DK (1) | DK353680A (es) |
ES (1) | ES494301A0 (es) |
FI (1) | FI802582A (es) |
GR (1) | GR69938B (es) |
HU (1) | HU182190B (es) |
IE (1) | IE50789B1 (es) |
IL (1) | IL60751A (es) |
MA (1) | MA18929A1 (es) |
NO (1) | NO155491C (es) |
NZ (1) | NZ194557A (es) |
PL (2) | PL132249B1 (es) |
PT (1) | PT71672B (es) |
YU (1) | YU207180A (es) |
ZA (1) | ZA805016B (es) |
ZW (1) | ZW19080A1 (es) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4440927A (en) * | 1981-06-19 | 1984-04-03 | Merck & Co., Inc. | Process for preparing inhibitors of 3-hydroxy-3-methylglutaryl coenzyme A reductase via a chiral synthon |
EP0068038B1 (en) * | 1981-06-29 | 1985-09-25 | Merck & Co. Inc. | (+)-(4r,6s)-(e)-6-(2-(4'-fluoro-3,3',5-trimethyl-(1,1'-biphenyl)-2-yl)ethenyl)-3,4,5,6-tetrahydro-4-hydroxy-2h-pyran-2-one, a process for preparing and a pharmaceutical composition containing the same |
US4588820A (en) * | 1984-06-11 | 1986-05-13 | Merck & Co., Inc. | Process for epimerization at C6 of 3,4,5,6-tetrahydro-2H-pyran-2-one |
US4647576A (en) * | 1984-09-24 | 1987-03-03 | Warner-Lambert Company | Trans-6-[2-(substitutedpyrrol-1-yl)alkyl]-pyran-2-one inhibitors of cholesterol synthesis |
DE3615620A1 (de) * | 1986-05-09 | 1987-11-12 | Hoechst Ag | 4(r)-substituierte 6(s)-phenoxymethyl-, 6(s)-(beta)-phenylaethyl-und 6(s)-(beta)-styryl-tetrahydropyran-2-one, ein hochstereoselektives verfahren zu ihrer herstellung, pharmazeutische praeparate auf basis dieser verbindungen und ihre verwendung |
US4897490A (en) * | 1987-02-25 | 1990-01-30 | Bristol-Meyers Company | Antihypercholesterolemic tetrazole compounds |
US4898949A (en) * | 1987-02-25 | 1990-02-06 | Bristol-Myers Company | Intermediates for the preparation of antihypercholesterolemic tetrazole compounds |
US5169976A (en) * | 1987-11-25 | 1992-12-08 | Pfizer Inc. | N-(biphenylmethyl)-3-hydroxyglutaramic acid and derivatives as hypocholesterolemic agents |
FI94339C (fi) | 1989-07-21 | 1995-08-25 | Warner Lambert Co | Menetelmä farmaseuttisesti käyttökelpoisen /R-(R*,R*)/-2-(4-fluorifenyyli)- , -dihydroksi-5-(1-metyylietyyli)-3-fenyyli-4-/(fenyyliamino)karbonyyli/-1H-pyrroli-1-heptaanihapon ja sen farmaseuttisesti hyväksyttävien suolojen valmistamiseksi |
US5093363A (en) * | 1989-08-22 | 1992-03-03 | Shionogi & Co., Ltd. | 2,4,6-substituted phenol derivatives |
JP3171931B2 (ja) * | 1992-06-02 | 2001-06-04 | 高砂香料工業株式会社 | (R)−(−)−4−シアノ−3−ヒドロキシ酪酸t−ブチルエステル及びその製造方法 |
IL129871A (en) * | 1994-05-06 | 2003-11-23 | Pharmacia & Upjohn Inc | Process for preparing 4-phenyl-substituted octanoyl-oxazolidin-2-one intermediates that are useful for preparing pyran-2-ones useful for treating retroviral infections |
RU2563831C1 (ru) * | 2014-10-13 | 2015-09-20 | Федеральное государственное бюджетное учреждение науки Иркутский институт химии им. А.Е. Фаворского Сибирского отделения Российской академии наук | Применение протатран 4-хлор-2-метилфеноксиацетата (хлоркрезацина) для угнетения активности холестеролэстеразы |
WO2016161085A1 (en) | 2015-04-01 | 2016-10-06 | Cedars-Sinai Medical Center | Anti-methanogenic lovastatin analogs or derivatives and uses thereof |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS53147073A (en) * | 1977-05-24 | 1978-12-21 | Sankyo Co Ltd | Mevalonolactone derivatives |
JPS5559180A (en) * | 1978-10-30 | 1980-05-02 | Sankyo Co Ltd | 4-hydroxy-2-pyrone ring compound, its preparation, and remedy for hyperlipemia comprising it as active constituent |
-
1980
- 1980-08-04 NZ NZ194557A patent/NZ194557A/en unknown
- 1980-08-04 IL IL60751A patent/IL60751A/xx unknown
- 1980-08-05 AU AU61085/80A patent/AU6108580A/en not_active Abandoned
- 1980-08-07 MA MA19129A patent/MA18929A1/fr unknown
- 1980-08-07 PT PT71672A patent/PT71672B/pt unknown
- 1980-08-11 KR KR1019800003182A patent/KR840002170B1/ko active
- 1980-08-12 GR GR62660A patent/GR69938B/el unknown
- 1980-08-12 CS CS805551A patent/CS219921B2/cs unknown
- 1980-08-14 ES ES494301A patent/ES494301A0/es active Granted
- 1980-08-14 AT AT80104807T patent/ATE16487T1/de not_active IP Right Cessation
- 1980-08-14 DD DD80223335A patent/DD152558A5/de unknown
- 1980-08-14 DE DE8080104807T patent/DE3071230D1/de not_active Expired
- 1980-08-14 EP EP80104807A patent/EP0024348B1/en not_active Expired
- 1980-08-14 NO NO802431A patent/NO155491C/no unknown
- 1980-08-15 YU YU02071/80A patent/YU207180A/xx unknown
- 1980-08-15 ZA ZA00805016A patent/ZA805016B/xx unknown
- 1980-08-15 HU HU802042A patent/HU182190B/hu not_active IP Right Cessation
- 1980-08-15 FI FI802582A patent/FI802582A/fi not_active Application Discontinuation
- 1980-08-15 DK DK353680A patent/DK353680A/da not_active Application Discontinuation
- 1980-08-15 CA CA000358416A patent/CA1137989A/en not_active Expired
- 1980-08-15 ZW ZW190/80A patent/ZW19080A1/xx unknown
- 1980-08-15 IE IE1732/80A patent/IE50789B1/en unknown
- 1980-08-15 JP JP11186880A patent/JPS5645470A/ja active Granted
- 1980-08-16 PL PL1980238108A patent/PL132249B1/pl unknown
- 1980-08-16 PL PL1980226285A patent/PL127979B1/pl unknown
Also Published As
Publication number | Publication date |
---|---|
JPH0257550B2 (es) | 1990-12-05 |
EP0024348A1 (en) | 1981-03-04 |
CS219921B2 (en) | 1983-03-25 |
NO155491C (no) | 1987-04-08 |
ZW19080A1 (en) | 1982-03-17 |
EP0024348B1 (en) | 1985-11-13 |
PL127979B1 (en) | 1983-12-31 |
DD152558A5 (de) | 1981-12-02 |
IE801732L (en) | 1981-02-17 |
IL60751A (en) | 1985-04-30 |
MA18929A1 (fr) | 1981-04-01 |
NZ194557A (en) | 1984-09-28 |
GR69938B (es) | 1982-07-21 |
JPS5645470A (en) | 1981-04-25 |
IL60751A0 (en) | 1980-10-26 |
NO802431L (no) | 1981-02-18 |
ATE16487T1 (de) | 1985-11-15 |
PT71672A (en) | 1980-09-01 |
YU207180A (en) | 1983-02-28 |
FI802582A (fi) | 1981-02-18 |
PT71672B (en) | 1982-01-22 |
KR840002170B1 (ko) | 1984-11-26 |
ES494301A0 (es) | 1981-07-16 |
IE50789B1 (en) | 1986-07-23 |
ZA805016B (en) | 1982-03-31 |
CA1137989A (en) | 1982-12-21 |
NO155491B (no) | 1986-12-29 |
KR830003465A (ko) | 1983-06-20 |
PL226285A1 (es) | 1981-03-27 |
HU182190B (en) | 1983-12-28 |
DK353680A (da) | 1981-02-19 |
AU6108580A (en) | 1981-02-19 |
DE3071230D1 (en) | 1985-12-19 |
PL132249B1 (en) | 1985-02-28 |
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