首页> 外国专利> Procedure for obtaining 3-ethyl-5-methyl 2,6-dimethyl-4- (3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate

Procedure for obtaining 3-ethyl-5-methyl 2,6-dimethyl-4- (3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate

机译:获得3-乙基-5-甲基2,6-二甲基-4-(3-硝基苯基)-1,4-二氢吡啶-3,5-二羧酸酯的步骤

摘要

New procedure for obtaining 3-ethyl-5-methyl 2,6-dimethyl- 4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate, in two stages. The obtaining of ethyl 2-(3- nitro)benzylideneacetoacetate from 3-nitrobenzaldehyde and ethyl acetoacetate in the presence of piperidine, glacial acetic acid and isopropanol, a second step in which the previous product is treated with methyl 3- aminocrotonate in the presence of activated alumina to give the title product. Advantages which are obtained by this procedure relative to the prior art: a) Processes carried out under rapid, smooth and simple conditions, giving products of high quality. b) The last step is carried out in a solid phase, avoiding traces of symmetrical dihydropyridines. c) Obtaining of the dihydropyridine without a solvent, minimum production of contaminating effluent. d) Use of recyclable basic or acid catalysts. e) Low cost in the processes, minimization of reagents and residues. f) Low environmental impact. IMAGE
机译:分两个阶段获得3-乙基-5-甲基2,6-二甲基-4-(3-硝基苯基)-1,4-二氢吡啶-3,5-二羧酸酯的新方法。在哌啶,冰醋酸和异丙醇的存在下,从3-硝基苯甲醛和乙酰乙酸乙酯中获得2-(3-硝基)苄叉基乙乙酸乙酯,第二步是在3-氨基苯甲酸甲酯存在下,用3-氨基巴豆酸甲酯处理先前的产物。活化的氧化铝得到标题产物。通过该程序相对于现有技术获得的优点:a)在快速,平稳和简单的条件下进行的过程,得到高质量的产品。 b)最后一步在固相中进行,避免了痕量对称的二氢吡啶。 c)在没有溶剂的情况下获得二氢吡啶,最小化污染废水的产生。 d)使用可回收的碱性或酸性催化剂。 e)流程成本低,将试剂和残留物降至最低。 f)对环境的影响小。 <图像>

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