Synthesis of 2-Substituted-6-amino-4, 5-dihydropyrimidine
The convenient synthesis of 2-substituted-6-amino-4, 5-dihydropyrimidine from the reaction of imidic ester with 3-aminopropionitrile was reported. Next, 2-phenyl- (V) and 2-(2-acylaminoethyl)-6-amino-4, 5-dihydropyrimidines were investigated to clarify their predominant form in the possible from the...
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Veröffentlicht in: | Chemical & pharmaceutical bulletin 1969/11/25, Vol.17(11), pp.2273-2278 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | The convenient synthesis of 2-substituted-6-amino-4, 5-dihydropyrimidine from the reaction of imidic ester with 3-aminopropionitrile was reported. Next, 2-phenyl- (V) and 2-(2-acylaminoethyl)-6-amino-4, 5-dihydropyrimidines were investigated to clarify their predominant form in the possible from the aspects of infrared spectra. Thus, it was found that V exists as the imino-form and 2-(2-acylaminoethyl)-6-amino-4, 5-dihydropyrimidines as the amino-form in the solid state. Further, it was described the synthesis of 3-acylaminopropionamidine possessing the heterocyclic ring for the purpose of potenciating the activity of benzamidopropionamidine which was studied previously. |
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ISSN: | 0009-2363 1347-5223 |
DOI: | 10.1248/cpb.17.2273 |