反应 #1909787

ord-a7e1308cf54448cca57929d0b63ed123

反应方程式

O=C(O)C1=C(O)C(Cl)C(O)(Cl)C=C1
3,4-dichloro-2,4-dihydroxybenzoic acid
COC(=O)[C@@H](N)Cc1ccccc1.Cl
L-phenylalanine methyl ester hydrochloride
CCN=C=NCCCN(C)C.Cl
WSC.HCl
On1nnc2ccccc21
HOBT
COC(=O)[C@H](Cc1ccccc1)NC(=O)c1cc(Cl)c(O)c(Cl)c1O
title compound
收率 63.1%
COC(=O)[C@H](Cc1ccccc1)NC(=O)c1cc(Cl)c(O)c(Cl)c1O
N-(3,5-Dichloro-2,4-dihydroxybenzoyl)-L-phenylalanine methyl ester
收率 63.1%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONThen, the mixture was post-treated in the same manner as in the above Example 1, (Step 5)

实验过程

To a solution of 3,4-dichloro-2,4-dihydroxybenzoic acid (17 g), L-phenylalanine methyl ester hydrochloride (19.8 g), WSC.HCl (17.6 g) and HOBT (12.4 g) in DMF (70 ml) was added dropwise triethylamine (12.8 ml) at room temperature, and the mixture was stirred for 16 hours. Then, the mixture was post-treated in the same manner as in the above Example 1, (Step 5) to give the title compound (18.32 g, yield 57%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: USRE039088E1uspto-grants-2006_05