HRID2119625
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
A mixture of 4-[(4-benzylphenyl)amino]-1-methyl-1H-pyrazole-5-carboxylic acid (EXAMPLE 11, step 1, 4.86 g, 15.81 mmol) in phosphorus oxychloride (40 ml) was refluxed for 3 h. After cooling to room temperature, the mixture was concentrated and dried in vacuo. The mixture was dissolved in ethyl acetate (300 ml), washed with water (100 ml) and saturated aqueous sodium bicarbonate (100 ml×2) and dried over magnesium sulfate. Removal of solvent gave the dark red residue, which was chromatographed on a column of silica gel eluting with ethyl acetate/hexane (1/3) to afford 3.86 g (79%) of the title compound as a yellow solid.
WORKUP
后处理
- temperaturewas refluxed for 3 h
- concentrationthe mixture was concentrated
- customdried in vacuo
- dissolutionThe mixture was dissolved in ethyl acetate (300 ml)
- washwashed with water (100 ml) and saturated aqueous sodium bicarbonate (100 ml×2)
- dry with materialdried over magnesium sulfate
- customRemoval of solvent
- customgave the dark red residue, which
- customwas chromatographed on a column of silica gel eluting with ethyl acetate/hexane (1/3)