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Synlett 1991; 1991(11): 821-823
DOI: 10.1055/s-1991-20890
DOI: 10.1055/s-1991-20890
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© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved.
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data processing and storage.Reduction of the Pyrimidine Ring: Regio- and Stereoselective Synthesis of 1,3-Diamine Derivatives
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Publikationsdatum:
07. März 2002 (online)
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1-Butyl-1,2-dihydropyrimidines 2 and 6,7,8,8a-tetrahydropyrrolo[1,2-a]pyrimidines 3 are reduced with an excess of sodium borohydride in methanol to produce stereoselectively N,N′ - and N,N-disubstituted 1,3-diamine derivatives 4 and 6, respectively. Partial reduction of 3 to fully saturated pyrrolo[1,2-a]pyrimidines 7 is accomplished using equimolecular amounts of sodium borohydride.