Synthesis of 2-(2-R1-Hydrazino)-5-(R2-benzyl)-2-thiazolines on the Basis of Meerweins Arylation Products of Allyl Isothiocyanate

Autor: Mykola I. Ganushchak, Mykola D. Obushak, Volodymyr V. Karpyak
Jazyk: angličtina
Rok vydání: 2003
Předmět:
Zdroj: Molecules, Vol 8, Iss 2, Pp 263-268 (2003)
Druh dokumentu: article
ISSN: 1420-3049
92503276
DOI: 10.3390/80200263
Popis: 3-Aryl-2-chloropropylisothiocyanates (1) are formed by interaction of arenediazonium chlorides with allyl isothiocyanate. Adducts 1 react with monoacylhydrazines to form 1-acyl-4-(3-aryl-2-chloropropyl)thiosemicarbazides (2a–d). Thiosemicarbazides 2a–d in the presence of bases selectively transform into 2-(2-R1-hydrazino)-5-(R2-benzyl)-2-thiazolines (3a–d).
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