Abstract
We have shown that as a result of reaction of phenylisocyanate with 2-benzyl- and 2-aryliminohexahydrothiazepines, the corresponding N-substituted N-tetrahydroazepinyl-N′-phenylureas are formed. In the case of isothiocyanates, on boiling in different solvents we obtained the products of the exchange reaction; and at room temperature, we also obtained substituted thioureas. We suggest a probable scheme for the process.
Similar content being viewed by others
References
R. F. Ambartsumova, M. G. Levkovich, and E. G. Mil'grom, Khim. Geterotsikl. Soedin., No. 1, 128 (1997).
D. N. Reinhoudt, Rec. Trav. Chim.,92, No. 1, 20 (1973).
T. Kato, N. Katagiri, U. Izumi, J. Miura, T. Jamazaki, and J. Hirai, Heterocycles,15, 399 (1981).
R. F. Ambartsumova and U. Mamatalieva, Uzb. Khim. Zh., No. 5, 35 (1991).
B. A. Kazanskii (ed.), Syntheses of Organic Compounds [Russian translation], Inostr. Lit, Moscow (1949), Vol. 9, p. 494.
S. Stankovsky and S. Kovac, Chem. Zvesti,28, 247 (1974).
G. D. Thorn and R. A. Ludwig, The Dithiocarbamates and Related Compounds, Elsevier, Amsterdam-New York (1962), p. 113.
Additional information
For communication 1, see [1].
Institute of Phytochemistry, Academy of Sciences of the Uzbekistan Republic, Tashkent 700170. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 416–422, March, 1997.
Rights and permissions
About this article
Cite this article
Ambartsumova, R.F., Levkovich, M.G. & Abdullaev, N.D. 1,3-thiazepines. 2. Reaction of 2-iminohexahydrothiazepines with phenylisocyanate and isothiocyanates. Chem Heterocycl Compd 33, 355–360 (1997). https://doi.org/10.1007/BF02253119
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF02253119