Synthesis of 2-[mercapto(cyano)methylene]-1,2,3,4-tetrahydro-quinazolin-4-ones and 2-amino-4-methylpyrazolo-[1,5-a]quinazolin-5(4H)-one
✍ Scribed by Judit Fleischer; Kálmán Takács; István Hermecz
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1997
- Tongue
- English
- Weight
- 248 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A series of 2‐[mercapto(cyano)methylene]‐1,2,3,4‐tetrahydroquinazolin‐4‐ones and 2‐amino‐4‐methylpyrazolo[1,5‐a]quinazolin‐5(4__H__)‐one were prepared from 2‐cyanomethylquinazolin‐4(3__H__)‐ones via α‐bromo derivatives 4 and amide oxime 8, respectively. The new compounds have been characterized by elemental analyses and ^1^H‐nmr, in some cases by ir and ^13^C‐nmr investigations.
📜 SIMILAR VOLUMES
## Abstract magnified image A novel series of 2,4‐disubstituted‐1,2,4‐triazolo[1,5‐__a__]quinazolin‐5(4__H__)‐ones were prepared by Dimroth rearrangement of their respective isomers namely 1,4‐disubstituted‐[1,2,4]triazolo[4,3‐__a__]‐quinazolin‐5(4__H__)‐ones. The latter were prepared __via__ new
## Abstract The reaction of 3‐__N__‐(2‐mercapto‐4‐oxo‐4__H__‐quinazolin‐3‐yl)acetamide (**1**) with hydrazine hydrate yielded 3‐amino‐2‐methyl‐3__H__‐[1,2,4]triazolo[5,1‐__b__]quinazolin‐9‐one (**2**). The reaction of **2** with __o__‐chlorobenzaldehyde and 2‐hydroxy‐naphthaldehyde gave the corresp