Microwave assisted synthesis of novel 6,7,8-trimethoxy N-substituted-4-aminoquinazoline compounds
✍ Scribed by Gang Liu; Lin Sun; Chunping Liu; Chunnuan Ji; Quanwu Wen; Songmei Ma
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2008
- Tongue
- English
- Weight
- 281 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
magnified image
A fast, efficient and convenient reaction of 6,7,8‐trimethoxy‐4‐chloroquinazoline and aryl (or benzyl) amines was achieved under microwave irradiation in isopropyl alcohol, providing a simple method for synthesis of novel 6,7,8‐trimethoxy N‐substituted‐4‐aminoquinazoline compounds in good yield in short time. The title compounds were evaluated for their in vitro anti‐proliferative activities against PC3 cell by MTT method.
📜 SIMILAR VOLUMES
## Abstract 4‐__N__,__N__‐Dimethylamino‐ and 4‐cycloamino‐5‐phenyl‐1,2,4‐triazole‐3‐thiones **1–13** have been synthesized from benzhydrazides and substituted methyl dithiocarbazates under various conditions including short microwave irradiations. The last method seemed faster than the classical re
Microwave Assisted Synthesis of Phenyl(2-phenyl-5,6,7,8-tetrahydro--4-quinolinyl)methanone and Its Derivatives. -The hitherto unreported title compounds (IV) are obtained from triketones (III) via an one-pot oxidative amination--cyclization-aromatization protocol. The reaction rate is promoted by mi