## Abstract Reaction of the 1‐substituted biguanides (I) with benzil (II) under microwave conditions affords the imidazolyl guanidine intermediates (III) as a mixture of tautomers within a few minutes.
An efficient microwave-assisted synthesis of 6,8-dihydroimidazo[1,2-a] [1,3,5] triazine derivatives
✍ Scribed by Mitra Matloobi; Hans Wolfgang Schramm
- Book ID
- 102343989
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2010
- Tongue
- English
- Weight
- 87 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.378
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✦ Synopsis
Abstract
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A simple, efficient, and general method has been developed for the synthesis of various 4‐substituted 2‐amino‐6,6‐diphenyl‐8‐aryl‐6,8‐dihydroimidazo[1,2‐a] [1,3,5] triazine‐7(4‐H)ones 3a, 3b, 3c, 3d, 3e, 3f, 3g, 3h, 3i, 3j, 3k, 3l, 3m, 3n, 3o, 3p, 3q, 3r, 3s, 3t, 3v. This involved condensation of 1‐(5‐oxo‐4,4‐diphenyl‐1‐aryl‐4,5‐dihydro‐1__H__‐imidazol‐2‐yl)guanidines 2a and 2b, themselves obtained from the reaction of aryl biguanides 1a/b with benzil, with the requisite carbonyl compounds. Both steps were performed using microwave heating in sealed vessels. J. Heterocyclic Chem., (2010).
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