期刊
CENTRAL EUROPEAN JOURNAL OF CHEMISTRY
卷 9, 期 1, 页码 143-148出版社
SCIENDO
DOI: 10.2478/s11532-010-0132-x
关键词
Hantzsch synthesis; 1,4-dihydropyridine; Ionic liquid; Catalysis; 1-butyl-4-methylpyridinium chloride
资金
- European Social Foundation (ESF) [2009/0197/1DP/1.1.1.2.0/09/APIA/VIAA/014, 2009/0138/1DP/1.1.2.1.2/09/IPIA/VIAA/004]
The synthesis of cationic amphiphilic 1,4-dihydropyridine derivative, potential gene delivery agent is achieved via an efficient multi-step sequence. The key step of this approach is a two-component Hantzsch type cyclisation of 3-oxo-2-[1-phenylmethylidene]-butyric acid dodecyl ester and 3-amino-but-2-enoic acid dodecyl ester utilising bis(2-hydroxyethyl)ether as a solvent and 1-butyl-4-methylpyridinium chloride as a catalyst. The 1,4-dihydropyridine derivative with long alkyl ester chains at positions 3 and 5 of the 1,4-DHP ring - 3,5-bis(dodecyloxycarbonyl)-2,6-dimethyl-4-phenyl-1,4-dihydropyridine was obtained in substantially higher yield with respect to classical Hantzsch synthesis. Bromination of this compound followed by nucleophilic substitution of bromine with pyridine gave the desired cationic amphiphilic 1,4-dihydropyridine.
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