反应详情
EQUATION
反应方程式
REACTANTS
反应物
Methanesulfonic acid
CH4O3S
2 次
L-Leucine, N-[(1,1-dimethylethoxy)carbonyl]-
C11H21NO4
tert-Butoxycarbonyl-D-leucine
C11H21NO4
1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride
C8H18ClN3
1H-Benzotriazol-1-ol--water (1/1)
C6H7N3O2
未命名化合物
未命名化合物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
Boc-Leu-Arg(Ts)-Pro-NHEt was prepared from Boc-Arg(Ts)-Pro-NHEt obtained in Example 1 and Boc-Leu by the same procedure as Example 1. To a solution composed of the compound (0.969 g) and dichloromethane (10 ml), methanesulfonic acid (0.78 g) was added at room temperature, and the resulting mixture was stirred at room temperature for 4 hours, thereby the Boc group was removed (reaction conversion ratio: 100.0%). After the reaction, triethylamine in an amount of the same molar equivalent as that of the added methanesulfonic acid was added thereto, and the resulting mixture was stirred for 15 minutes. After Boc-D-Leu (0.40 g) and HOBt monohydrate (0.33 g) were added to the thus obtained dichloromethane solution of Leu-Arg(Ts)-Pro-NHEt, the reaction solution was cooled with ice. Then, EDC hydrochloride (0.42 g) was added thereto, and the resulting mixture was stirred for 1 hour. Subsequently, the temperature of the mixture was raised to room temperature and the mixture was stirred for 15 hours, thereby performing a condensation reaction (reaction conversion ratio: 100.0%).
WORKUP
后处理
- additionwas added at room temperature
- customthe Boc group was removed
- custom(reaction conversion ratio: 100.0%)
- additionwas added
- stirringthe resulting mixture was stirred for 15 minutes
- temperaturethe reaction solution was cooled with ice
- stirringthe resulting mixture was stirred for 1 hour
- temperatureSubsequently, the temperature of the mixture was raised to room temperature
- stirringthe mixture was stirred for 15 hours
- customa condensation reaction (reaction conversion ratio: 100.0%)