Studying the synthesis of 4-tert-butyl-1,3-dihydroimidazol-2-ones and their corresponding thiones
✍ Scribed by Yasser M. Loksha; Erik B. Pedersen; Ahmed A. El-Barbary; Mahmoud A. El-Badawi; Claus Nielsen
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2003
- Tongue
- English
- Weight
- 87 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
4‐tert‐Butyl‐1,3‐dihydroimidazol‐2‐ones and 1,3‐dihydroimidazol‐2‐thiones were synthesized from 1‐amino‐3,3‐dimethylbutanone and subjected to alkylation reactions. The latter compounds were S‐alkyl‐ated with iodoacetamide under alkaline conditions. The N^1^ N^3^‐unsubstituted derivative was iodinated and subsequently alkylated with alkylation reagents which previously have been used for the synthesis of anti‐HTV active imidazoles. Unfortunately, the present products were devoid of activity against HTV.
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## Abstract Aromatic‐substituted derivatives of 1,3,2‐diazaphospholidin‐4‐ones **2a–g** were readily prepared from 1,3‐diaryl glycinamides **1** by the reaction with hexaethylphosphoric triamide. Their chemical transformation was selectively effected with different thionation reagents to afford thi
## 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
The title compound BDI is prepared on multigram scale, so clean that highly efficient in-situ double alkylations are feasible, in which the sequence of addition of the two either by resolution of the precursor 2-tert-butylimidazolidin-4-one (from glycine amide and pivalaldehyde) through different el