反应 #806286

ord-115106d942d844c887401f5d53bd7a13

反应方程式

CC(C)(C)OC(=O)CNC(=O)[C@H](NC(=O)OCc1ccccc1)c1ccccc1
(R)-N-Benzyloxycarbonyl-α-[N-(t-butoxycarbonylmethyl)carbamoyl]benzylamine
CC(C)(C)OC(=O)CNC(=O)[C@H](N)c1ccccc1
title compound
收率 99.0%
CC(C)(C)OC(=O)CNC(=O)[C@H](N)c1ccccc1
(R)-α-[N-(t-Butoxycarbonylmethyl)carbamoyl]benzylamine
收率 99.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤The reaction mixture was filtered through diatomaceous earth
  2. 2
    其他the solvents were evaporated

实验过程

(R)-N-Benzyloxycarbonyl-α-[N-(t-butoxycarbonylmethyl)carbamoyl]benzylamine (Method 4; 12.8 g, 32.2 mmol) was dissolved in EtOH (99%, 200 ml) and toluene (50 ml). Pd/C (10%, 0.65 g) was added and hydrogenation was performed at atmospheric pressure for 5.5 hours at room temperature. The reaction mixture was filtered through diatomaceous earth and the solvents were evaporated to give the title compound (8.4 g, 99%). NMR (600 MHz, CDCl3): 1.45 (s, 9H), 3.93 (m, 2H), 4.54 (s, 1H), 7.31–7.42 (m, 5H), 7.51 (brs, 1H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07132416B2uspto-grants-2006_11