反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a solution of 1-amino-4-bromo-6-fluoro-isoquinoline (0.0395 g, 0.164 mmol) in DMF (1 mL) are added 6,6-Dimethyl-3-trifluoromethyl-1,5,6,7-tetrahydro-indazol-4-one (0.046 g, 0.2 mmol) and NaH (0.008 g, 0.2 mmol). The reaction mixture is microwaved at 120° C. for 40 min, cooled to RT, and treated with NH4Cl (satd. aq, 2 mL). The aqueous phase is extracted with EtOAc (2×). The combined organic layers are washed with brine, and dried over MgSO4. The solvent is evaporated and the residue is dried under vacuum. Purification of the crude material using a Biotage column (10% MeOH/CH2Cl2) affords 0.039 g (53%) of 1-(1-Amino-4-bromo-isoquinolin-6-yl)-6,6-dimethyl-3-trifluoromethyl-1,5,6,7-tetrahydro-indazol-4-one. LC/MS m/z=454 [M+H]+.
WORKUP
后处理
- customThe reaction mixture is microwaved at 120° C. for 40 min
- extractionThe aqueous phase is extracted with EtOAc (2×)
- washThe combined organic layers are washed with brine
- dry with materialdried over MgSO4
- customThe solvent is evaporated
- customthe residue is dried under vacuum
- customPurification of the crude material