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N-[2-(4-特戊酰氧基苯磺酰胺基)苯甲酰基]甘氨酸苄酯的合成
引用本文:孙晋瑞,国大亮. N-[2-(4-特戊酰氧基苯磺酰胺基)苯甲酰基]甘氨酸苄酯的合成[J]. 中国药物化学杂志, 2006, 16(2): 79-81,111
作者姓名:孙晋瑞  国大亮
作者单位:山东省医药工业研究所,山东,济南,250100
摘    要:目的合成西维来司钠(sivelestat sodium)的关键中间体N—[2-(4-特戊酰氧基苯磺酰胺基)苯甲酰基]甘氨酸苄酯(1)。方法先以特戊酸、氯化亚砜、对羟基苯磺酸为原料,经酯化、苯磺酸成酰氯得到对位特戊酰氧基苯磺酰氯(4);再以甘氨酸、苄醇、邻硝基苯甲酰氯为原料经酯化、酰氨化、还原得到N-(2-氨基苯甲酰基)甘氨酸苄酯(7);将4和7两中间体缩合得1。结果及结论本方法原料廉价易得,条件温和易控,收率较高,适合工业化生产。

关 键 词:药物化学  化合物制备  化学合成  N-[2-(4-特戊酰氧基苯磺酰胺基)苯甲酰基]甘氨酸苄酯  西维来司钠
文章编号:1005-0108(2006)02-0079-03
收稿时间:2005-11-04
修稿时间:2005-11-04

Synthesis of N-[2-(4-trimethylacetoxybenzenesulphonamino) benzoyl]glycine benzyl ester
SUN Jin-rui,GUO Da-liang. Synthesis of N-[2-(4-trimethylacetoxybenzenesulphonamino) benzoyl]glycine benzyl ester[J]. Chinese Journal of Medicinal Chemistry, 2006, 16(2): 79-81,111
Authors:SUN Jin-rui  GUO Da-liang
Abstract:Aim To synthesize the key intermediate of sivelestat sodium,N-[2-(4-trimethylacetoxybenzenesulphonamino)benzoyl]g lycine benzyl ester.Method Trimethylacetic acid,thionyl chioride and p-hydroxybenzenesulfonic acid was treated by esterification,sulfonyl c hloride formation to give trimethylacetoxybenzenesulfonic chloride (4. Glycine,benzyl alcohol and o-nitrobenzoyl chloride was treated by esterifi cation,acylamination and reduction to give N-(2-aminobenzoyl)glycine benzy l alcohol ester.The target compound was obtained by condensa tion between and.Results and co nclusion The raw materials in this route is cheap,and the reaction condi tion is easy to control.Yield is higher and this method can be applied in indust ry production.
Keywords:medicinal chemistry  compound preparation  chemical s ynthesis  N-[2-(4-trimethylacetoxybenzenesulphonamino)benzoyl]glycine b enzyl ester  sivelestat sodium
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