反应详情
EQUATION
反应方程式
REACTANTS
反应物
5-Bromo-2-chlorobenzoic acid
C7H4BrClO2
Diisopropylethylamine
C8H19N
Methanaminium, N-[(1H-benzotriazol-1-yloxy)(dimethylamino)methylene]-N-methyl-, hexafluorophosphate(1-) (1:1)
C11H16F6N5OP
4-Amino-N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanine methyl ester
C15H22N2O4
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a mixture of 4-amino-N-[(1,1-dimethylethoxy)carbonyl)-L-phenylalanine methyl ester (20 mmol, 5.88 g), 2-chloro-5-bromobenzoic acid (22 mmol, 5.18 g) and HBTU (22 mmol, 8.34 g) in DMF (70 mL) was added diisopropylethylamine (50 mmol, 8.7 mL) at room temperature. The suspension was stirred for 48 h at which time TLC analysis of the mixture indicated the absence of starting material. Then, the mixture was diluted with water (100 mL) and the solids were collected by filtration and washed with water (150 mL). After air drying, the crude product was purified by silica gel column chromatography to obtain 1.02 g (10%) of a white solid: mp 158-161° C. HR MS (C22H24BrClN2O5): Ob, 533.0442. Calcd mass, 533.0455 (M+Na).
WORKUP
后处理
- filtrationthe solids were collected by filtration
- washwashed with water (150 mL)
- customAfter air drying
- customthe crude product was purified by silica gel column chromatography