Some New 4-Aryl-2-thiazolylhydrazones. -Three series of new 4-aryl-2-thiazolylhydrazones [cf. (III), (V), (VII)] are synthesized by condensation of appropriate thiosemicarbazones with phenacyl bromides (II). Some of the title compounds show biological activity on plants in the laboratory tests, but
Synthesis and some reactions of 4-carboxy-2-thiazolylhydrazones
β Scribed by Z. A. Bredikhina; B. I. Buzykin; Yu. P. Kitaev
- Publisher
- Springer US
- Year
- 1991
- Tongue
- English
- Weight
- 687 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0009-3122
No coin nor oath required. For personal study only.
β¦ Synopsis
Vl)
. Pyrrolidone (0.94 g, 11 mmole) and phosphorus oxychloride (1 ml, 11 mmole) were added to a solution of IV (3.45 g, 10 mmole) in dry dichloroethane (30 ml) and the reaction mixture was heated for 1.5 h. It was cooled, saturated aqueous sodium acetate solution (30 ml) added, and refluxed for 20 min. After cooling, the organic layer was separated, washed with water, and the dichloroethane distilled off. The residue was treated with alcohol, heated to reflux, cooled, and the precipitate filtered off to give VI (2 g). Found: M + 366. Calculated: M 366.
8-Hydrβ’xy-7-pheny
was prepared similarly to VI. Found: M + 394. Calculated: M 394.
LITERATURE CITED
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