HRID418294
反应详情
EQUATION
反应方程式
REACTANTS
反应物
HCID962
Water
H2O
HCID75771
1-Hydroxybenzotriazole
C6H5N3O
HCID81531
Diisopropylethylamine
C8H19N
HCID1910189
Pyrazolo[1,5-a]pyrimidine-3-carboxylic acid
C7H5N3O2
HCID2554578
未命名化合物
HCID2733084
Methanaminium, N-[(1H-benzotriazol-1-yloxy)(dimethylamino)methylene]-N-methyl-, hexafluorophosphate(1-) (1:1)
C11H16F6N5OP
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a solution of 1-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazine (may be prepared as described in Description 1) (200 mg, 0.680 mmol) in DMF (5 ml) was added pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (111 mg, 0.680 mmol), HOBT.H2O (104 mg, 0.680 mmol) and HBTU (258 mg, 0.680 mmol). Finally DIPEA (0.356 ml, 2.039 mmol) was added and the reaction mixture was stirred at rt for 20 hours. Solvent was removed by evaporation, the crude partitioned between DCM (50 ml) and saturated aq. sodium bicarbonate (50 ml), the DCM layer collected, dried (hydrophobic frit) and evaporated. MDAP purification yielded the title compound (317 mg) as an off-white solid.
WORKUP
后处理
- customSolvent was removed by evaporation
- customthe crude partitioned between DCM (50 ml) and saturated aq. sodium bicarbonate (50 ml)
- customthe DCM layer collected
- customdried (hydrophobic frit)
- customevaporated
- customMDAP purification