Volume 29, Issue 1
Preparative Organic Chemistry
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ChemInform Abstract: Reaction of 2-Phenylaminothiazoline with α-Haloketones.

A. M. DEMCHENKO

A. M. DEMCHENKO

Chernigovskii tekhnol. inst., Chernigov 250027, Ukraine

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V. A. CHUMAKOV

V. A. CHUMAKOV

Chernigovskii tekhnol. inst., Chernigov 250027, Ukraine

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A. N. KRASOVSKII

A. N. KRASOVSKII

Chernigovskii tekhnol. inst., Chernigov 250027, Ukraine

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V. V. PIROZHENKO

V. V. PIROZHENKO

Chernigovskii tekhnol. inst., Chernigov 250027, Ukraine

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M. O. LOZINSKII

M. O. LOZINSKII

Chernigovskii tekhnol. inst., Chernigov 250027, Ukraine

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First published: 24 June 2010

Abstract

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ChemInform Abstract

The reaction of α-haloketones (II) with aminothiazoline (I) proceeds regioselectively by attack of the halide at the exocyclic nitrogen atom of the aminothiazoline (I) to give the imidazo[2,1-b]thiazolinium bromides (III). The structure of the bromides is supported by spectroscopic and chemical methods.

chemical structure image

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