反应 #216924

ord-8fd3275186e24e7c832681c10c4167b9

反应方程式

Clc1ccc2c(c1)Cc1ccccc1[C@@H]1CNCCN21
(14bR)-8-chloro-1,2,3,4,10,14b-hexahydrodibenzo[c,f]pyrazino[1,2-a]azepine
O=C1c2ccccc2C(=O)N1CCBr
N-(2-bromoethyl)phthalimide
O=C1c2ccccc2C(=O)N1CCN1CCN2c3ccc(Cl)cc3Cc3ccccc3[C@@H]2C1
title compound
收率 47.0%
O=C1c2ccccc2C(=O)N1CCN1CCN2c3ccc(Cl)cc3Cc3ccccc3[C@@H]2C1
(14bR)-8-Chloro-2-(2-phthalimidoethyl)-1,2,3,4,10,14b-hexahydrodibenzo[c,f]pyrazino[1,2-a]azepine
收率 47.0%

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Following a procedure similar to that described in Preparation 14(a), but using (14bR)-8-chloro-1,2,3,4,10,14b-hexahydrodibenzo[c,f]pyrazino[1,2-a]azepine and N-(2-bromoethyl)phthalimide, the title compound was obtained in a yield of 47%.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05470851uspto-grants-1995_11