WO1987002662A3 - Analogues heterocycliques de mevalonolactone et leurs derives, procedes de production et utilisation en tant que produits pharmaceutiques - Google Patents
Analogues heterocycliques de mevalonolactone et leurs derives, procedes de production et utilisation en tant que produits pharmaceutiques Download PDFInfo
- Publication number
- WO1987002662A3 WO1987002662A3 PCT/EP1986/000598 EP8600598W WO8702662A3 WO 1987002662 A3 WO1987002662 A3 WO 1987002662A3 EP 8600598 W EP8600598 W EP 8600598W WO 8702662 A3 WO8702662 A3 WO 8702662A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- 3alkyl
- hydrogen
- group
- formula
- pharmaceuticals
- 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.)
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—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
- C07D207/30—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
- C07D207/32—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
- 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
- C07D207/337—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Composés de formule (I) dans laquelle Ra est un groupe -X-Z, Rb est R2, Rc est R3, Rd est R4 et Y est un groupe (III) ou Ra est R1, Rb est un groupe -X-Z, Rc est R2, Rd est R3 et Y est O, S ou un groupe (IV); R1, R2, R3 et R4 sont chacun indépendamment C1-6alkyle ne contenant pas d'atome de carbone asymétrique, C3-7cycloalkyle ou un anneau (V) ou, dans le cas R3 et R4, également hydrogène, ou, lorsque Y est O ou S, R3 et représenté par (VI) où R17 est hydrogène ou C1-3alkyle et R18 et R19 sont indépendamment hydrogène, C1-3alkyle ou phényle; chaque R5 est indépendamment hydrogène, C1-3alkyle, n-butyle, i-butyle, t-butyle, C1-3alkoxy, n-butoxy, i-butoxy, trifluorométhyle, fluoro, chloro, bromo, phényle, phénoxy ou benzyloxy; chaque R6 est indépendamment hydrogène, C1-3alkyle, C1-3alkoxy, trifluorométhyle, fluoro, chloro, bromo, phénoxy ou benzyloxy, et chaque R7 est indépendamment hydrogène, C1-2alkyle, C1-2alkoxy, fluoro ou chloro, à condition que chaque anneau A ne puisse présenter qu'un élément parmi trifluorométhyle, phénoxy ou benzyloxy, X est (CH2)m ou (CH2)qCH=CH-(CH2)q, m vaut 0, 1, 2 ou 3 et les deux q valent 0 ou l'un d'entre eux vaut 0 et l'autre vaut 1, Z présente la formule (II) où R9 est hydrogène ou C1-3alkyle. Ces composés se présentent sous la forme d'un acide libre, ou sous la forme d'un ester ou d'un delta-lactone de celui-ci ou sous une forme de sel, selon les besoins, et sont indiqués pour être utilisés comme produits pharmaceutiques notamment en tant qu'agents hypolipoprotéinémiques et anti-artériosclérotiques.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU865313A HUT48208A (en) | 1985-10-25 | 1986-10-21 | Process for producing heterocyclic analogues of mevalolactone derivatives and pharmaceutical compositions comprising such compounds |
| KR1019870700553A KR900001212B1 (ko) | 1985-10-25 | 1986-10-21 | 메바로노락톤 및 그것의 유도체의 헤테로사이클릭 유사체 및 그것의 생산방법 및 약학적인 그것의 용도 |
| FI872299A FI872299A0 (fi) | 1985-10-25 | 1987-05-25 | Heterocykliska analoger av mevalonolaktoner och deras derivat, foerfaranden foer deras framstaellning och deras anvaendning som farmaceutiska medel. |
| DK321887A DK321887D0 (da) | 1985-10-25 | 1987-06-24 | Mevalonolactonanaloge |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US79119885A | 1985-10-25 | 1985-10-25 | |
| US791,198 | 1985-10-25 | ||
| US81666486A | 1986-01-07 | 1986-01-07 | |
| US816,664 | 1986-01-07 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO1987002662A2 WO1987002662A2 (fr) | 1987-05-07 |
| WO1987002662A3 true WO1987002662A3 (fr) | 1987-12-17 |
Family
ID=27121116
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP1986/000598 Ceased WO1987002662A2 (fr) | 1985-10-25 | 1986-10-21 | Analogues heterocycliques de mevalonolactone et leurs derives, procedes de production et utilisation en tant que produits pharmaceutiques |
Country Status (12)
| Country | Link |
|---|---|
| EP (1) | EP0221025A1 (fr) |
| KR (1) | KR900001212B1 (fr) |
| AU (1) | AU598775B2 (fr) |
| CA (1) | CA1278794C (fr) |
| DK (1) | DK321887D0 (fr) |
| FI (1) | FI872299A0 (fr) |
| HU (1) | HUT48208A (fr) |
| IL (1) | IL80403A (fr) |
| NZ (1) | NZ218045A (fr) |
| PL (1) | PL154130B1 (fr) |
| PT (1) | PT83610B (fr) |
| WO (1) | WO1987002662A2 (fr) |
Families Citing this family (98)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
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| NO881411L (no) * | 1987-04-14 | 1988-10-17 | Bayer Ag | Substituerte pyrroler. |
| US5091378A (en) * | 1987-05-22 | 1992-02-25 | E. R. Squibb & Sons, Inc. | Phosphorus-containing HMG-CoA reductase inhibitors, new intermediates and method |
| DE3722806A1 (de) * | 1987-07-10 | 1989-01-19 | Hoechst Ag | 7-(1h-pyrrol-3-yl)-substituierte 3,5-dihydroxy-hept-6-ensaeuren, 7-(1h-pyrrol-3-yl)-substituierte 3,5-dihydroxy-heptansaeuren, ihre entsprechenden (delta)-lactone und salze, verfahren zu ihrer herstellung ihre verwendung als arzneimittel, pharmazeutische praeparate und zwischenprodukte |
| DE3817808A1 (de) * | 1987-07-21 | 1989-02-02 | Bayer Ag | Verfahren zur herstellung von 2-substituierten pyrrolen |
| US4822799A (en) * | 1988-01-27 | 1989-04-18 | Sandoz Pharm. Corp. | Pyrazolopyridine analogs of mevalonolactone and derivatives thereof useful for inhibiting cholesterol biosynthesis in mammals |
| NO890988L (no) * | 1988-03-24 | 1989-09-25 | Bayer Ag | Disubstituerte pyrroler. |
| EP0339342A1 (fr) * | 1988-04-23 | 1989-11-02 | Bayer Ag | N-aminopyrrols N-substitués |
| EP0352575A3 (fr) * | 1988-07-28 | 1991-08-21 | Bayer Ag | Pyrroles annelés substitués |
| DE3826814A1 (de) * | 1988-08-06 | 1990-02-08 | Hoechst Ag | Neue 6-fluor-3,5-dihydroxycarbonsaeuren und deren derivate, verfahren zu ihrer herstellung, ihre verwendung als arzneimittel, pharmazeutische praeparate und zwischenprodukte |
| US5506219A (en) * | 1988-08-29 | 1996-04-09 | E. R. Squibb & Sons, Inc. | Pyridine anchors for HMG-CoA reductase inhibitors |
| DE3832570A1 (de) * | 1988-09-24 | 1990-03-29 | Hoechst Ag | 7-substituierte derivate der 3,5-dihydroxyhept-6-insaeure, verfahren zur ihrer herstellung, ihre verwendung als arzneimittel, sowie zwischenprodukte |
| IT1237470B (it) * | 1988-10-03 | 1993-06-07 | Glaxo Group Ltd | Derivati di imidazolo, procedimenti per produrli e composizioni farmaceutiche che li contengono |
| 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 |
| AU637408B2 (en) * | 1989-10-10 | 1993-05-27 | Glaxo Group Limited | Substituted N-vinyl imidazole derivatives. |
| IT1237792B (it) * | 1989-12-21 | 1993-06-17 | Zambon Spa | Composti attivi come inibitori dell'enzima hmg-coa reduttasi |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3168527A (en) * | 1962-06-14 | 1965-02-02 | Parke Davis & Co | 1-aryl-5-(p-fluorophenyl)-pyrrole-2-propionic acid compounds |
| DE1695941A1 (de) * | 1966-04-25 | 1971-05-13 | Upjohn Co | Verfahren zur Herstellung von 5-gliedrigen N-Heterocyclen,die im Ring ungesaettigt sind |
| FR2164857A1 (fr) * | 1971-12-23 | 1973-08-03 | Continental Pharma | |
| US4035394A (en) * | 1976-02-24 | 1977-07-12 | Morton-Norwich Products, Inc. | 5-Phenyl-2-furanyl-oxo or-hydroxy alkanoic acids and ethyl esters as gastric acid antisecretory agents |
| EP0117228A1 (fr) * | 1983-01-24 | 1984-08-29 | Sandoz Ag | Analogues de mévalonolactone et leur dérivés, leur procédé de production, compositions pharmaceutiques les contenant ainsi que leur utilisation comme médicaments |
| EP0125415A1 (fr) * | 1983-03-16 | 1984-11-21 | BASF Aktiengesellschaft | Procédé de production de pyrroles |
| AT377255B (de) * | 1982-06-22 | 1985-02-25 | Richter Gedeon Vegyeszet | Verfahren zur herstellung von 1-alkyl- bzw. 1,4-dialkyl-1h-pyrrol-2-essigsaeure-alkylestern |
| EP0155524A1 (fr) * | 1984-03-01 | 1985-09-25 | A. Nattermann & Cie. GmbH | Composé omega-aryl-alkylthianyliques, leur procédé de préparation et produits pharmaceutiques les contenant |
| WO1986000307A2 (fr) * | 1984-06-22 | 1986-01-16 | Sandoz Ag | Analogues pyrazole de la mevalonolactone et leurs derives, leurs procedes de preparation et leur utilisation |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3168532A (en) * | 1963-06-12 | 1965-02-02 | Parke Davis & Co | 1, 5-diarylpyrrole-2-propionic acid compounds |
| WO1984002131A1 (fr) * | 1982-11-22 | 1984-06-07 | Sandoz Ag | Produits analogues de mevalolactone et leurs derives, leurs procedes de production, compositions pharmaceutiques les contenant ainsi que leur utilisation en tant que produits pharmaceutiques |
| AU599580B2 (en) * | 1984-12-04 | 1990-07-26 | Sandoz Ag | Indene analogs of mevalonolactone |
-
1986
- 1986-10-21 KR KR1019870700553A patent/KR900001212B1/ko not_active Expired
- 1986-10-21 EP EP86810470A patent/EP0221025A1/fr not_active Withdrawn
- 1986-10-21 WO PCT/EP1986/000598 patent/WO1987002662A2/fr not_active Ceased
- 1986-10-21 AU AU65994/86A patent/AU598775B2/en not_active Ceased
- 1986-10-21 HU HU865313A patent/HUT48208A/hu unknown
- 1986-10-23 NZ NZ218045A patent/NZ218045A/xx unknown
- 1986-10-23 IL IL80403A patent/IL80403A/xx unknown
- 1986-10-23 PT PT83610A patent/PT83610B/pt not_active IP Right Cessation
- 1986-10-24 CA CA000521333A patent/CA1278794C/fr not_active Expired - Lifetime
- 1986-10-24 PL PL1986262032A patent/PL154130B1/pl unknown
-
1987
- 1987-05-25 FI FI872299A patent/FI872299A0/fi not_active Application Discontinuation
- 1987-06-24 DK DK321887A patent/DK321887D0/da not_active Application Discontinuation
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3168527A (en) * | 1962-06-14 | 1965-02-02 | Parke Davis & Co | 1-aryl-5-(p-fluorophenyl)-pyrrole-2-propionic acid compounds |
| DE1695941A1 (de) * | 1966-04-25 | 1971-05-13 | Upjohn Co | Verfahren zur Herstellung von 5-gliedrigen N-Heterocyclen,die im Ring ungesaettigt sind |
| FR2164857A1 (fr) * | 1971-12-23 | 1973-08-03 | Continental Pharma | |
| US4035394A (en) * | 1976-02-24 | 1977-07-12 | Morton-Norwich Products, Inc. | 5-Phenyl-2-furanyl-oxo or-hydroxy alkanoic acids and ethyl esters as gastric acid antisecretory agents |
| AT377255B (de) * | 1982-06-22 | 1985-02-25 | Richter Gedeon Vegyeszet | Verfahren zur herstellung von 1-alkyl- bzw. 1,4-dialkyl-1h-pyrrol-2-essigsaeure-alkylestern |
| EP0117228A1 (fr) * | 1983-01-24 | 1984-08-29 | Sandoz Ag | Analogues de mévalonolactone et leur dérivés, leur procédé de production, compositions pharmaceutiques les contenant ainsi que leur utilisation comme médicaments |
| EP0125415A1 (fr) * | 1983-03-16 | 1984-11-21 | BASF Aktiengesellschaft | Procédé de production de pyrroles |
| EP0155524A1 (fr) * | 1984-03-01 | 1985-09-25 | A. Nattermann & Cie. GmbH | Composé omega-aryl-alkylthianyliques, leur procédé de préparation et produits pharmaceutiques les contenant |
| WO1986000307A2 (fr) * | 1984-06-22 | 1986-01-16 | Sandoz Ag | Analogues pyrazole de la mevalonolactone et leurs derives, leurs procedes de preparation et leur utilisation |
Also Published As
| Publication number | Publication date |
|---|---|
| KR870700602A (ko) | 1987-12-30 |
| KR900001212B1 (ko) | 1990-02-28 |
| IL80403A0 (en) | 1987-01-30 |
| FI872299A7 (fi) | 1987-05-25 |
| PL154130B1 (en) | 1991-07-31 |
| PT83610B (pt) | 1989-05-31 |
| PT83610A (en) | 1986-11-01 |
| EP0221025A1 (fr) | 1987-05-06 |
| IL80403A (en) | 1990-09-17 |
| NZ218045A (en) | 1990-03-27 |
| DK321887A (da) | 1987-06-24 |
| HUT48208A (en) | 1989-05-29 |
| CA1278794C (fr) | 1991-01-08 |
| AU6599486A (en) | 1987-05-19 |
| AU598775B2 (en) | 1990-07-05 |
| WO1987002662A2 (fr) | 1987-05-07 |
| DK321887D0 (da) | 1987-06-24 |
| FI872299A0 (fi) | 1987-05-25 |
| PL262032A1 (en) | 1988-07-21 |
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