反应详情
EQUATION
反应方程式
REACTANTS
反应物
Benzenesulfonic acid, 3-amino-5-chloro-4-methyl-
C7H8ClNO3S
Diisopropylethylamine
C8H19N
3H-1,2,3-Triazolo[4,5-b]pyridine, 3-hydroxy-
C5H4N4O
Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)
C10H15F6N6OP
未命名化合物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
After 2 ml of DMF and 0.52 ml (3 mmol) of DIEA were added to 303 mg (1 mmol) of Boc-Glu-OtBu hydrochloride, 221 mg (1 mmol) of 3-amino-5-chloro-4-methylbenzenesulfonic acid, 160 mg (1.3 mmol) of HOAt and 410 mg (1.3 mmol) of HATU, the mixture was stirred at room temperature overnight. The reaction solution was diluted in water-acetonitrile and purified in accordance with the purification step A to give the protected form of the product. The protected product obtained was dissolved in 5 ml of trifluoroacetic acid and stirred for 2 hours. After the solvent was removed by distillation, the mixture was purified in accordance with the purification step A to give the title compound.
WORKUP
后处理
- custompurified in accordance with the purification step A
- customto give the protected form of the product
- customThe protected product obtained
- stirringstirred for 2 hours
- customAfter the solvent was removed by distillation
- customthe mixture was purified in accordance with the purification step A