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Reactions of 6-aminopyrimidines with 2-dimethylaminomethylenetetralone. Regiospecific Synthesis Of 5,6-Dihydrobenzo [h]pyrimido [4,5-b] quinolines
✍ Scribed by Jairo Quiroga; Braulio Insuasty; Henry Insuasty; Rodrigo Abonia; Antonio Ortíz; Adolfo Sánchez; Manuel Nogueras
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2001
- Tongue
- English
- Weight
- 34 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
Benzo[h]pyrimido[4,5‐b]quinolines (3) have been synthesized via a regiospecific cyclocondensation reaction between 6‐aminopyrimidines (1) and 2‐dimethylaminomethylentetralone hydrochloride (2). The linear structure of the final compounds were determined by nmr measurements, especially by ^1^H,^1^H, ^1^H,^13^C COSY and DEPT experiments.
📜 SIMILAR VOLUMES
The reaction of 6-aminopyrimidines \(1 \mathbf{a}, \mathbf{b}\) with dimedone (2) and p-substituted benzaldehydes \(\mathbf{3 a}\)-d in ethanol afforded in all cases new regiospecific synthesis of tricyclic, linear 5-aryl-5,6,7,8,9,10-hexahydropyrimido[4,5-b]quinolines 4a-h in good yields. The linea
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