Synthesis and X-ray crystal structure of the calcium channel antagonist: dimethyl 1,4-dihydro-2,6-dimethyl-4-[4′-(4H-4-oxo-1-benzopyran-2-yl)phenyl]-3,5-pyridine dicarboxylate
✍ Scribed by Meral Tunçbilek; Süheyla Özbey; Engin Kendi; Engin Yıldırım; Kevser Erol; Rahmiye Ertan
- Book ID
- 114019530
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 139 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0014-827X
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## Abstract The Hantzsch condensation of the heteroarylcarboxaldehydes 3a‐c with alkyl acetoacetates 4a‐c and alkyl 3‐aminocrotonates 5a‐b afforded the respective dialkyl 1,4‐dihydro‐2,6‐dimethyl‐4‐(heteroaryl)‐pyridine‐3,5‐dicarboxylates 6a‐f possessing a C‐4 4‐quinolinyl, 8‐quinolinyl or 1‐oxido‐
We report the synthesis and X-ray crystal structure of 1,4-dihydro-2,6-dimethyl-4-(2'isopropylphenyl)-3,5-pyridine-dicarboxylic acid dimethyl ester (4), an analogue of the 1,4dihydropyridine calcium channel antagonist, nifedipine. Solution state NOE data indicate the presence of both rotameric forms