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Reactions with hydrazonoyl halides XXVIII*: Synthesis of some 2-thiazolylimino-2,3-dihydro-1,3,4-thiadiazoles

✍ Scribed by Abdou O. Abdelhamid; Nadia A. Abdel-Riheem; Nabil M. Hassan


Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
163 KB
Volume
11
Category
Article
ISSN
1042-7163

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✦ Synopsis


Hydrazonoyl halides have been caused

to react with each of methyl 5-ethoxycarbonyl-4-methylthiazole-2-aminothiocarbamate, benzyl 5-ethoxycarbonyl-4-methylthiazole-2-aminothiocarbamate, and 5-ethoxycarbonyl-4-methylthiazol-2-ylphenylthiourea in the presence of triethylamine to give 2-imino-(5-ethoxycarbonyl-4-methyl)thiazolyl-2,3-dihydro-1,3, 4-thiadiazoles in good yields. Structures of the new compounds were elucidated on the basis of elemental analyses, spectral data, and alternative methods of synthesis whenever possible.


πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Reactions with Hydr
✍ N. M. HASSAN; A. O. ABDELHAMID πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 36 KB

Reactions with Hydrazonoyl Halides. Part 16. A Convenient Synthesis of 1,4-Benzothiazine (VII), Triazolo[4,3-a]benzimidazole (V), Thiazolo[3,2-a]benzimidazole (III) and 2,3-Dihydro-1,3,4-thiadiazole Derivatives ((IX), (XI)) -[by condensation reactions of hydrazonoyl bromide (I)]. -(HASSAN, N.