ChemInform Abstract: 1,3-Thiazepines. Part 2. Reaction of 2-Iminohexahydrothiazepines with Phenyl Isocyanate and Isothiocyanates.
โ Scribed by R. F. AMBARTSUMOVA; M. G. LEVKOVICH; N. D. ABDULLAEV
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 30 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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โฆ Synopsis
1,3-Thiazepines. Part 2. Reaction of 2-Iminohexahydrothiazepines with Phenyl Isocyanate and Isothiocyanates.
-Reaction of the iminothiazepines (I) with phenyl isocyanate (II) gives the expected ureas (III) in good yields. In contrast, reaction with aryl isothiocyanates in refluxing toluene produces only substitution products (cf. (V)). Under more mild conditions (acetone, room temperature), unexpectedly substituted thioureas are obtained, e.g. compound (VII)/(VIII).
๐ SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
Part 4. Reaction of 2-Iminothiazepines with Methyl Acrylate. Crystal and Molecular Structure of 2-Phenylimino-3-(ฮฒ-methoxycarbonylethyl)-and 2-Benzyliminohexahydro-1,3thiazepines. -Reaction of 2-iminothiazepines (I) with methyl acrylate (II) proceeds at the endocyclic nitrogen to give the 2-imino-3