反应详情
EQUATION
反应方程式
REACTANTS
反应物
Water
H2O
1-Hydroxybenzotriazole
C6H5N3O
Diisopropylethylamine
C8H19N
Pyrazolo[1,5-a]pyrimidine-3-carboxylic acid
C7H5N3O2
Methanaminium, N-[(1H-benzotriazol-1-yloxy)(dimethylamino)methylene]-N-methyl-, hexafluorophosphate(1-) (1:1)
C11H16F6N5OP
未命名化合物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a solution of (3R)-3-methyl-1-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazine (may be prepared as described in Description 10) (80.0 mg, 0.259 mmol) in DMF (4 ml) was added pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (42.3 mg, 0.259 mmol), HOBT.H2O (39.7 mg, 0.259 mmol), HBTU (98 mg, 0.259 mmol) and DIPEA (0.136 ml, 0.778 mmol) and the reaction mixture was stirred at rt for 1.5 hours. The DMF was evaporated in vacuo then DCM (5 ml) was added and the whole washed with saturated aq. NaHCO3 solution (5 ml), dried on a phase separation cartridge and evaporated in vacuo. The crude material was dissolved in MeCN/DMSO 1:1 and purified by MDAP to give the title compound (100 mg).
WORKUP
后处理
- customThe DMF was evaporated in vacuo
- additionDCM (5 ml) was added
- washthe whole washed with saturated aq. NaHCO3 solution (5 ml)
- customdried on a phase separation cartridge
- customevaporated in vacuo
- dissolutionThe crude material was dissolved in MeCN/DMSO 1:1
- custompurified by MDAP