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恩他卡朋的合成 被引量:4

Synthesis of entacapone
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摘要 目的用改进的方法合成及纯化恩他卡朋,提高产率。方法以3,4-二羟基-5-硝基苯甲醛和N,N-二乙基-氰基酰胺为原料,在弱碱性条件下经过克脑文格尔反应生成2-氰基-N,N-二乙基-3-(3,4-二羟基-5-硝基苯基)丙烯酰胺,然后对顺反异构体进行纯化,最后进行红外光谱分析,元素分析,X-射线粉末衍射分析。结果所合成的终产物图谱与标品一致。 OBJECTIVE In order to increase product rate, new way has been taken to prepare and purify entacapone. METHOD 3,4-dihydroxy-5-nitro-benzaldehyde was used to react with N, N-diethylcyanoacetamide, between which taking place knoevengal reaction in base condition, the crude product 2-cyano-N, N-diethyl-3-( 3,4dihydroxy-5-nitrophenl) acrylamide was purified to obtain E-isomer, the result product was analyzed, such as element analysis, X-ray power diffraction analysis and infrared spectrum. RESULT The spectrum of result product is the same as standard compound.
出处 《中国现代应用药学》 CAS CSCD 北大核心 2005年第6期456-456,共1页 Chinese Journal of Modern Applied Pharmacy
关键词 恩他卡朋 合成 几何异构 纯化 entacapone synthesis gemetric isomer purify
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