In:
Zeitschrift für Naturforschung B, Walter de Gruyter GmbH, Vol. 62, No. 1 ( 2007-1-1), p. 104-110
Abstract:
The reaction of 6-aminouracil (1) with the appropriate α,β -unsaturated ketones, gave the corresponding pyrido[2,3-d]pyrimidin-2,4-diones 3, 6, 8 and 10, respectively. Treatment of 1 with salicylaldehyde, 6-carboethoxy-3,5-diphenyl-2-cyclohexenone (13) or 2,6- bis(phenylmethylidene)cyclohexanone (15) afforded the corresponding pyrimido[4,5-d] quinoline- 2,4-diones 12, 14 and 16, respectively. Furthermore, a pyrido[2,3-d]pyrimidine incorporating 3,2’- bis(quinoline) derivative 18 was synthesized. Annulation of pyrido[2,3-d] pyrimidine with pyrazole or imidazole moieties was achieved via reaction of 1 with benzylidene derivatives of pyrazolone, imidazolone or 3-carboethoxycoumarin (23) to give 21, 22 and 24, respectively.
Type of Medium:
Online Resource
ISSN:
1865-7117
,
0932-0776
DOI:
10.1515/znb-2007-0115
Language:
English
Publisher:
Walter de Gruyter GmbH
Publication Date:
2007
detail.hit.zdb_id:
2078109-X
detail.hit.zdb_id:
124635-5
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