Synthesis of 2-amino-1,4-dihydro-4-quinolinones and diaminomethylene meldrum's acids derivatives as potential potassium channel openers
✍ Scribed by Béanéadicte Erb; Benoît Rigo; Bernard Pirotte; Daniel Couturier
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2002
- Tongue
- English
- Weight
- 158 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Starting from 5‐bismethylthiomethylene Meldrum's acid, the synthesis of 5‐diaminomethylene Meldrum's acids and 2‐aminoquinolone derivatives, structurally related to potassium channels openers pinacidil and diazoxide, is described.
📜 SIMILAR VOLUMES
## Abstract Starting from 2‐thioxoquinazolin‐4‐one, the synthesis of 2‐amino‐4(3__H__)‐one derivatives, structurally related to potassium channels openers pinacidil and diazoxide, is described.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
Synthesis of Some 4-[3' or 4'-(4H-4-Oxo-1-benzopyran-2-yl)phenyl]-1,4-dihydropyridine Derivatives as Potential Calcium Channel Antagonists. -A series of new flavonoid derivatives bearing a dihydropyridine moiety on the phenyl ring [cf. (IV), (VII), 23 examples] are prepared. Compound (IVa) exhibits