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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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