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 |
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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). |
Databáze: | Directory of Open Access Journals |
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