反应详情
EQUATION
反应方程式
REACTANTS
反应物
Hydrochloric Acid
ClH
未命名化合物
Sodium Hydroxide
HNaO
L-Tyrosine, methyl ester, hydrochloride (1:1)
C10H14ClNO3
Diisopropylethylamine
C8H19N
1-Cyclohexyl-2-(furan-3-yl)-1H-benzimidazole-5-carboxylic acid
C18H18N2O3
O-(Benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate
C11H16BF4N5O
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
The carboxylic acid of example 2 (0.075 g, 0.24 mmol) and TBTU (1.2 equiv., 0.29 mmol, 0.093 g) were dissolved in DMF (0.5 mL) and DIEA (5 equiv., 1.2 mmol, 0.21 mL) was added followed by tyrosine methyl ester hydrochloride (1.2 equiv., 0.29 mmol, 0.036 g). The mixture was stirred 30 min at room temperature. The reaction mixture was added drop-wise to 1 N NaOH (10 mL) and the mixture stirred until complete hydrolysis of the methyl ester (as determined by HPLC analysis). The pH of the solution was then adjusted to 5-6 by drop-wise addition of 1 N HCl. The gray precipitate that formed was collected by filtration, washed with water and dried (125 mg). The solid was further purified by reversed-phase HPLC using 0.1% TFA—0.1% TFA in acetonitrile gradients to give after lyophilisation, the TFA salt of the title compound as a white amorphous solid (35 mg).
WORKUP
后处理
- customThe gray precipitate that formed
- filtrationwas collected by filtration
- washwashed with water
- customdried (125 mg)
- customThe solid was further purified by reversed-phase
- customto give after lyophilisation