Abstract
The crystal and molecular structure of the title compound, obtained as a result of intramolecular cyclization of 5,5-diphenyl-2-carboxymethylmercaptohydantoin, has been determined from X-ray diffractometer data. The finalR was 0.049 for 1869 reflections. The conformation of the molecule was found to approximate to the conformations of other similar compounds, but owing to the presence of a C=O group in the thiazol ring, important differences in conjugated bonds system were observed.
Similar content being viewed by others
References
Chaudhary, H. S., Panda, C. S., and Pujari, H. K. (1970)Indian J. Chem. 8, 10.
Fetter, J., Horsanyi, K., Nyitrai, J., and Lempert, K. (1970)Acta Chim. Budapest 78, 325.
Harhash, A. H., Elnagdi, M. H., Sobhy, E. M., and Foda, K. M. (1975)Indian J. Chem. 13, 238.
Karolak-Wojciechowska, J., and Kieć-Kononowicz, K. (1987)J. Crystallogr. Spectrosc. Res. 17, 485.
Karolak-Wojciechowska, J., Mikołajczyk, M., Zatorski, A., Kieć-Kononowicz, K., and Zejc, A. (1985)Tetrahedron 41, 4593.
Kieć-Kononowicz, K. (1988) Unpublished results.
Kieć-Kononowicz, K., and Zejc, A. (1980)Pol. J. Chem. 54, 11, 2217.
Kieć-Kononowicz, K., Zatorski, A., and Karolak-Wojciechowska, J. (1988)Phosphorus and Sulfur.
Shalaby, A. F. A., Daboun, H. A., and Abde Aziz, M. A. (1976)Z. Naturforsch. 31b, 111.
Shalaby, A. F. A., Daboun, H. A., and Abdel Aziz, M. A. (1977)Z. Naturforsch. 32b, 948.
Wong, M. G., Define, I. A., and Andrews, P. R. (1986)J. Med. Chem. 29, 562.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Kieć-Kononowicz, K., Karolak-Wojciechowska, J. & Kwiatkowski, W. Reaction of 5,5-diphenyl-2-thiohydantoin with ethyl chloroacetate: Synthesis and crystal and molecular structure of 2,3,5,6-tetrahydroimidazo-[2,1-b]-thiazol-3,6-dione. Journal of Crystallographic and Spectroscopic Research 18, 563–573 (1988). https://doi.org/10.1007/BF01161149
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF01161149