Reactions of cyclic oxalyl compounds,part 29: A simple synthesis of functionalized 1H-pyrimidines |
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Authors: | Behzat Altural Yunus Akcamur Emin Saripinar Ismail Yildirim Gert Kollenz |
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Institution: | (1) Fen Edebiyat Faculty, Erciyes University, TR-38039 Kayseri, Turkey;(2) Institute of Organic Chemistry, Isotope Department, University of Graz, A-8010 Graz, Austria |
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Abstract: | Summary 4-Benzoyl-5-phenylfuran-2,3-dione (1) and the semicarbazones2, ureas and thioureas6, respectively, combine with loss of water and carbondioxide yielding the 1H-pyrimidine derivatives3 and7, respectively, in moderate yields (30–75%). Hydrolysis of3 b leads to the 1-amino-pyrimidine-2-one4.Cordially dedicated to o. Univ.-Prof. Dr. Hans Junek on the occasion of his 60th birthday |
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Keywords: | 5-Benzoyl-1-methyleneamino-4-phenyl-1H-pyrimidine-2-ones 1-Alkyl-5-benzoyl-4-phenyl-1H-pyrimidine-2-ones 1 4 5-Substituted pyrimidine-2-thiones Cyclocondensation reactions |
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