Basicities of thiazole heterocyclic compounds and the reaction of 3-methyl-2-methylimino-Δ4-thiazolines with ethyl bromoacetate and 2-bromoacetophenone
✍ Scribed by Dong Chan Kim; Kyung Ho Yoo; Kye Jung Shin; Sang Woo Park; Dong Jin Kim
- Book ID
- 102892162
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1997
- Tongue
- English
- Weight
- 537 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
The p__K__~a~′s of several thiazole heterocyclic compounds have been determined and represent products with significantly high values. Because of their high basicities, sometimes these compounds were able to act as not only nucleophiles but also strong organic bases. 4‐Substituted‐3‐methyl‐2‐methylimino‐Δ^4^‐thiazolines 5a‐d reacted with ethyl bromoacetate in refluxing benzene, giving the corresponding N‐alkylated salts 8a‐d, while the products obtained from the reaction with 2‐bromoacetophenone in the presence of base were pyrrolothiazines 10b‐d.
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## 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 reactions of ethyl 2-oxoindoliden-3-ylidene cyanoacetate (2a) and of 3-dicyanoethylideneindoliden-2-one (2b) with phenols and amines have been reported. 0 1996 John Wiley & Sons, Inc. a$-Unsaturated nitriles are highly reactive reagents and have been extensively utilized in heterocyclic synthesi