Preparation method of imidocarb dipropionate and intermediate thereof
The invention discloses a preparation method of imidocarb dipropionate and an intermediate thereof and belongs to the technical field of chemical pharmacy. According to the method, m-nitrobenzonitrilereacts with ethylenediamine with sodium sulfide taken as a catalyst; palladium on carbon-ammonium fo...
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Format: | Patent |
Sprache: | chi ; eng |
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Zusammenfassung: | The invention discloses a preparation method of imidocarb dipropionate and an intermediate thereof and belongs to the technical field of chemical pharmacy. According to the method, m-nitrobenzonitrilereacts with ethylenediamine with sodium sulfide taken as a catalyst; palladium on carbon-ammonium formate reduction is performed; a product and urea are subjected to condensation reaction, so that imidazole phenylurea dihydrochloride can be obtained; dissociated imidazole phenylurea reacts with propionic acid, so that the imidazole phenylurea dipropionate can be obtained. The method has the advantages o reduced wastes, cheap and easily available raw materials, simple operation, high product yield, simple process operation and high safety, and is suitable for industrial production.
本发明公开了一种二丙酸咪唑苯脲及其中间体的制备方法。属于化学制药技术领域。方法是将间硝基苯甲腈以硫化钠为催化剂与乙二胺反应,再经过钯碳甲酸铵还原,与尿素缩合反应制得咪唑苯脲二盐酸盐,游离出咪唑苯脲与丙酸反应制得二丙酸咪唑苯脲。本发明减少了废弃物的产生,原料廉价易得,操作简便,产品收率高,工艺操作简便,安全性高,适合工业化生产。 |
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