【药物名称】SGB-1534
化学结构式(Chemical Structure):
参考文献No.46469
标题:Phenylpiperazine derivatives
作者:Nagano, H.; et al. (Chugai Pharmaceutical Co. Ltd.)
来源:EP 0089065; JP 58159480; US 4578465
合成路线图解说明:

This compound can be obtained by two related ways: 1) By cyclization of 1-(2-methoxyphenyl)-4-[2-(2-aminobenzoyl)amino-ethyl]piperazine (I) with trichloromethyl chloroformate, with triethylamine as condensing agent and methylene chloride as solvent. 2) By cyclization of 1-(2-methoxyphenyl)-4-[2-(2-aminobenzoyl)amino-ethyl]piperazine (I) with urea by heating at 180 C in DMF.

参考文献No.75168
标题:SGB-1534
作者:Casta馿r, J.; Serradell, M.N.; Mannhold, R.
来源:Drugs Fut 1985,10(12),993
合成路线图解说明:

This compound can be obtained by two related ways: 1) By cyclization of 1-(2-methoxyphenyl)-4-[2-(2-aminobenzoyl)amino-ethyl]piperazine (I) with trichloromethyl chloroformate, with triethylamine as condensing agent and methylene chloride as solvent. 2) By cyclization of 1-(2-methoxyphenyl)-4-[2-(2-aminobenzoyl)amino-ethyl]piperazine (I) with urea by heating at 180 C in DMF.

Drug Information Express,Drug R&D,Chemical Database,Patent Search.
Copyright © 2006-2024 Drug Future. All rights reserved.Contact Us