CS258579B1 - (2R,SS,10aS,10bS)-5-Benzyl-3,6-dioxo-10b-hydroxy-2-karboxy-8-methoxy-2-methyl-2,3,5,6,9,10,10a,10b-oktahydro-8H-oxazolo/3,2-a/- pyrrolo/2,1-c/pyrazin a způsob jeho výroby - Google Patents
(2R,SS,10aS,10bS)-5-Benzyl-3,6-dioxo-10b-hydroxy-2-karboxy-8-methoxy-2-methyl-2,3,5,6,9,10,10a,10b-oktahydro-8H-oxazolo/3,2-a/- pyrrolo/2,1-c/pyrazin a způsob jeho výroby Download PDFInfo
- Publication number
- CS258579B1 CS258579B1 CS8610030A CS1003086A CS258579B1 CS 258579 B1 CS258579 B1 CS 258579B1 CS 8610030 A CS8610030 A CS 8610030A CS 1003086 A CS1003086 A CS 1003086A CS 258579 B1 CS258579 B1 CS 258579B1
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- benzyl
- dioxo
- pyrazine
- hydroxy
- methoxy
- Prior art date
Links
Landscapes
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Řešení se týká (2R,5S,10aS,10bS)- -5-benzyl-3,6-dioxo-10b-hydroxy-2-karboxy- -8-methoxy-2-methyl-2,3,5,6,9,10,10a,10b- -oktahydro-8H-oxazolo/3,2-a/pyrrolo/2,1-c/- pyrazinu a způsobu jeho výroby, vyznačujícího se tím, že se do reakce uvede (3S,8aS)- -3-benzyl-6-hydroxy-l,4-dioxo-l,2,3,4,6,- 7,8,8a-oktahydropyrrolo/1,2-a/pyrazin a methanol za přítomnosti katalytického množství kyseliny, načež se vzniklý 6-methoxyderivát uvede do reakce s ethylesterchloridem kyseliny (S)-2-benzyloxy- -2-methylmalonové a nestálý meziprodukt se katalytickou debenzylací a basickou hydrolysou převede na produkt. Připravená sloučenina je syntetickým prekursorem farmaceuticky využitelných látek.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS8610030A CS258579B1 (sk) | 1986-12-28 | 1986-12-28 | (2R,SS,10aS,10bS)-5-Benzyl-3,6-dioxo-10b-hydroxy-2-karboxy-8-methoxy-2-methyl-2,3,5,6,9,10,10a,10b-oktahydro-8H-oxazolo/3,2-a/- pyrrolo/2,1-c/pyrazin a způsob jeho výroby |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS8610030A CS258579B1 (sk) | 1986-12-28 | 1986-12-28 | (2R,SS,10aS,10bS)-5-Benzyl-3,6-dioxo-10b-hydroxy-2-karboxy-8-methoxy-2-methyl-2,3,5,6,9,10,10a,10b-oktahydro-8H-oxazolo/3,2-a/- pyrrolo/2,1-c/pyrazin a způsob jeho výroby |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CS1003086A1 CS1003086A1 (en) | 1987-12-17 |
| CS258579B1 true CS258579B1 (sk) | 1988-08-16 |
Family
ID=5447656
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS8610030A CS258579B1 (sk) | 1986-12-28 | 1986-12-28 | (2R,SS,10aS,10bS)-5-Benzyl-3,6-dioxo-10b-hydroxy-2-karboxy-8-methoxy-2-methyl-2,3,5,6,9,10,10a,10b-oktahydro-8H-oxazolo/3,2-a/- pyrrolo/2,1-c/pyrazin a způsob jeho výroby |
Country Status (1)
| Country | Link |
|---|---|
| CS (1) | CS258579B1 (sk) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108467398A (zh) * | 2018-05-29 | 2018-08-31 | 中国科学院烟台海岸带研究所 | 一种二酮哌嗪类化合物及其制备和应用 |
-
1986
- 1986-12-28 CS CS8610030A patent/CS258579B1/sk unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108467398A (zh) * | 2018-05-29 | 2018-08-31 | 中国科学院烟台海岸带研究所 | 一种二酮哌嗪类化合物及其制备和应用 |
| CN108467398B (zh) * | 2018-05-29 | 2020-06-23 | 中国科学院烟台海岸带研究所 | 一种二酮哌嗪类化合物及其制备和应用 |
Also Published As
| Publication number | Publication date |
|---|---|
| CS1003086A1 (en) | 1987-12-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SU776557A3 (ru) | Способ получени оптически активных антрациклинонов | |
| EP0109047A1 (en) | Total synthesis of antitumor antibiotics | |
| EP1280771B1 (de) | Neue prodrugs von 6-hydroxy-2,3-dihydro-1h-indolen, 5-hydroxy-1,2-dihydro-3h-pyrrolo 3,2-e]indolen und 5-hydroxy-1,2-dihydro-3h-benzo e]indolen sowie von 6-hydroxy-1,2,3,4-tetrahydro-benzo f]chinolin-derivaten für eine selektive krebstherapie | |
| EP0340064B1 (fr) | Benzodiazépines, leur procédé et intermédiaires de préparation et leurs applications en thérapeutique | |
| Tietze et al. | A novel approach in drug discovery: synthesis of estrone–talaromycin natural product hybrids | |
| US4977144A (en) | Imidazo[4,5-b]pyridine derivatives as cardiovascular agents | |
| MC1969A1 (fr) | Procedes pour preparer des composes antitumoraux,formulation pharmaceutique contenant ces composes,leurs utilisations en medecine et pharmacie,et composes intermediaires pour leur preparation | |
| US3652569A (en) | Ergonine ergoptine and the 1-methyl and 9 10-dihydro derivatives thereof | |
| SU910118A3 (ru) | Способ получени N @ -глюкофуранозид-6-ил-N @ -нитрозомочевины | |
| EP1042326B1 (fr) | Nouveaux derives de l'acronycine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent | |
| Tadano et al. | Synthesis of (-)-8a-epi-swainsonine,(1S, 2R, 8R, 8aS)-octahydro-1, 2, 8-indolizinetriol. | |
| JPS63303991A (ja) | エピポドフイロトキシングルコシドの窒素含有誘導体 | |
| CN112441982A (zh) | 一种盐酸咪达唑仑糖浆杂质a和杂质b及其用途 | |
| Maekawa et al. | meta-Substituent effects on the photocyclization of aryl-substituted N-acyl-α-dehydroalanine derivatives | |
| Rao et al. | A new route to annelated dihydrofurofurans. Synthesis of 6, 8-dideoxyversicolorin A | |
| KR820000419B1 (ko) | 니트로소-우레아 유도체의 제조방법 | |
| KR20000010893A (ko) | 마피아 포에티다(mappia foetida)에서 분리한캄토테신골격화합물 및 이들의 신규한 치료제 및 의약품기질로서의 용도 | |
| GB2036744A (en) | Eburnane derivatives | |
| US4474967A (en) | 8-Deutero and 8-tritio-substituted derivatives of D-4S-6-fluoro-spiro-[chroman-4,4'-imidazolidine]-2',5'-dione | |
| Jung et al. | Synthesis of fully functionalized intermediates for the bottom half of the 4-acyloxymethyl milbemycin antibiotics (1) | |
| Kalaus et al. | Synthesis of Vinca alkaloids and related compounds. 37. Some new reactions of (.+-.)-C-norquebrachamine and its derivatives | |
| Marquez et al. | 1, 3-Diazepinones. 1. Synthesis of 5-hydroxyperhydro-1, 3-diazepin-2-one | |
| US6458792B1 (en) | Compounds | |
| US4895854A (en) | Antitumor alkaloids | |
| CA2220995C (fr) | Nouveaux derives 7,12-dioxa-benzo¬a|anthraceniques substitues, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |