反应 #216925

ord-a5f1b35e691846eeb854bb8182d97120

反应方程式

c1ccc2c(c1)Cn1cccc1[C@@H]1CNCCN21
(14bS)-1,2,3,4,10,14b-hexahydropyrazino[1,2-a]pyrrolo[2,1-c][1,4]benzodiazepine
O=C1c2ccccc2C(=O)N1CCBr
N-(2-bromoethyl)phthalimide
O=C1c2ccccc2C(=O)N1CCN1CCN2c3ccccc3Cn3cccc3[C@@H]2C1
title compound
O=C1c2ccccc2C(=O)N1CCN1CCN2c3ccccc3Cn3cccc3[C@@H]2C1
(14bS)-2-(2-Phthalimidoethyl)-1,2,3,4,10,14b-hexahydropyrazino[1,2-a]pyrrolo[2,1-c][1,4]benzodiazepine

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 (14bS)-1,2,3,4,10,14b-hexahydropyrazino[1,2-a]pyrrolo[2,1-c][1,4]benzodiazepine and N-(2-bromoethyl)phthalimide, the title compound was obtained in a quantitative yield.

来源

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