Abstract
A new scheme was developed for the synthesis of 2,4-dimethy1-5,6-dihydro-6-bromomethylthieno[2,3-d]pyrimidine by bromination of the corresponding 5-allyl-6-mercaptopyrimidine. It is shown that when the bromomethyl derivative is treated with sodium methoxide a molecule of hydrogen bromide is split out to give 2,4,6-trimethylthieno[2,3-d]pyrimidine. The structures of the synthesized compounds were proved by PMR spectroscopy and mass spectrometry.
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R. G. Melik-Ogandzhanyan, R. G. Mirzoyan, and A. A. Aroyan, Arm. Khim, Zh., 28, 53 (1975).
R. G. Melik-Ogandzhanyan, A. S. Gapoyan, V. É. Khachatryan, V. S. Mirzoyan, Zh. S. Manukyan, and S. A. Papoyan, Arm. Khim. Zh., 33, 102Q (1980).
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See [1] for Communication 55.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 118–120, January, 1982.
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Melik-Ogandzhanyan, R.G., Gapoyan, A.S., Khachatryan, V.É. et al. Pyrimidine derivatives. 56. New method for the synthesis of thieno[2,3-d]pyrimidine. Chem Heterocycl Compd 18, 100–102 (1982). https://doi.org/10.1007/BF00513299
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DOI: https://doi.org/10.1007/BF00513299