New efficient approach for the synthesis of 2-alkyl(aryl) substituted 4H-pyrido[1,2-a]pyrimidin-4-ones
✍ Scribed by Helio G. Bonacorso; Fernando J. Righi; Isadora R. Rodrigues; Cleber A. Cechinel; Michelle B. Costa; Arci D. Wastowski; Marcos A. P. Martins; Nilo Zanatta
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2006
- Tongue
- English
- Weight
- 79 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
in 45 -80 % yield from the reaction of β-alkoxyvinyl trichloromethyl ketones with 2-aminopyridine under mild conditions, is then reported.
📜 SIMILAR VOLUMES
## Abstract Alkylation of 2‐hydroxy‐4__H__‐pyrido[1,2‐__a__]pyrimidin‐4‐one (**1**) was investigated under solid–liquid phase transfer catalysis conditions (PTC), using tetrabutylammonium bromide and potassium carbonate. The reaction with alkyl halides led to the formation of various 2‐alkoxy produ
## Abstract We report the condensation of substituted 2‐aminopyridines 5 with β‐ketocarboxylic esters in polyphosphoric acid. In this reaction were obtained together with the target compounds, 4__H__‐pyrido[1,2‐__a__]pyrirnidin‐4‐ones 6 also the pyridin‐2‐ones 7. All the compounds 7 were tested for
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