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-(3-trifluoromethyl-phenyl)-4,5-dihydro-1H-pyrazol-3-ylamine hydrochloride salt (200 mg, 0.88 mmol) (Example 3A) in dioxane (50 mL) was added triethylamine (0.069 mL, 0.88 mmol) followed by 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ) (200 mg, 0.88 mmol). The mixture was stirred at room temperature for 24 h and then poured onto dichloromethane. 2N hydrochloric acid was added and the organics extracted with 2N hydrochloric acid (3×50 mL). The acid layer was basified with 10N potassium hydroxide and extracted with dichloromethane (3×50 mL). The combined organics were dried (Na2SO4), filtered and evaporated to dryness. The residue dissolved in diethyl ether and 1M hydrochloric acid in diethyl ether was added to form a brown solid which was collected and dried (171 mg, 86%). MS (ES) m/z: 228.1 [M+H].
WORKUP
后处理
- additionpoured onto dichloromethane
- extractionthe organics extracted with 2N hydrochloric acid (3×50 mL)
- extractionextracted with dichloromethane (3×50 mL)
- dry with materialThe combined organics were dried (Na2SO4)
- filtrationfiltered
- customevaporated to dryness
- dissolutionThe residue dissolved in diethyl ether
- addition1M hydrochloric acid in diethyl ether was added
- customto form a brown solid which
- customwas collected
- customdried (171 mg, 86%)