Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5266852 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
A convenient synthesis of a series of pyrido[3,2-e][1,4]-diazepine-2,5-diones 8 and pyrido[2,3-e][1,4]diazepine-2,5-diones 9, is reported using the condensation of α-amino acid methyl ester derivatives with 1H-pyrido[3,2-d][1,3]oxazine-2,4-dione and 1H-pyrido[2,3-d][1,3]oxazine-2,4-dione. Compounds 8 and 9 were also synthesized by peptide coupling of α-amino acid methyl ester derivatives with β-amino acids (2 or 3) followed by the cyclisation in tetrahydrofuran with sodium hydride (NaH).
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Abderrahman El Bouakher, Hélène Laborie, Mina Aadil, Ahmed El Hakmaoui, Said Lazar, Mohamed Akssira, Marie-Claude Viaud-Massuard,