Synthesis of semicarbazones and thiosemicarbazones of 1-(2-benzothiazolon-3-yl) propanones
β Scribed by A. Ts. Antonova; D. Simov; V. B. Kalcheva
- Publisher
- Springer US
- Year
- 1989
- Tongue
- English
- Weight
- 220 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0009-3122
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β¦ Synopsis
Semi-and thiosemicarbazones were synthesized by the reaction of l-(2-benzothiazolon-3-yl)propanones with semi-and thiosemicarbazide, These compounds are more active in stimulating plant growth than the starting propanones.
Systems that contain two potentially biologically active segments usually display valuable biological activity.
In the present work we discuss the synthesis of such types of compounds, viz., the semicarbazones and the thiosemicarbazones, which usually show pronounced biological properties [i, 2]; they are derived from the benzothiazolonyl ketones, which are knownfor their physiological activity [3,4]. Indeed biological tests have shown that activ ity of these compounds in regulating plant growth is stronger [5] than that of the starting ketones [6].
Compounds (II) and (III) were obtained by the reaction of equimolar amounts of 1-(2benzothiazolonyl) propanones (I) and semi-or thiosemicarbazide in 68-97% yield (Table i).
π SIMILAR VOLUMES
A series of substituted N-(3-methylpyridin-2-yl) semicarbazones was designed and synthesized to meet the structural requirements essential for anticonvulsant activity. The structures of all the synthesized compounds were confirmed by means of spectral and elemental analysis. All the compounds were e
## Abstract Ten new (5βchloroβ2(3H)βbenzothiazolonβ3βyl)propanamide derivatives have been synthesized. The compounds were tested for antinociceptive activity by tail clip, tail flick, hot plate and writhing test by using aspirin and dipyrone as standards. Among these compounds, 1β[3β(5βchloroβ2(3H)