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 solution of 0.100 g (0.25 mmol) of 6-(2,6-dichlorophenyl)-8-ethyl-2-methanesulfonyl-8H-pyrido[2,3-d]pyrimidin-7-one of Example 68 and 0.061 g (0.50 mmol) of 4-methoxyaniline in 0.5 mL of dimethylformamide was heated at reflux for 10 minutes. Three drops of water were added. Crystals separated on inducement. An additional 3 drops of water were added to precipitate additional tacky solid. After decantation, the solid was triturated with 0.5 mL of ethyl acetate and 0.5 mL of petroleum ether. The solids were filtered and washed with 50% ethyl acetate/petroleum ether and dried; wt 0.080 g. Purification was effected by filtering an ethyl acetate solution through a layer of silica gel. Concentration of the filtrate to 1 mL volume yielded pure crystalline product; wt 0.033 g; mp 213°-215° C.
WORKUP
后处理
- temperatureat reflux for 10 minutes
- customCrystals separated on inducement
- additionAn additional 3 drops of water were added
- customto precipitate additional tacky solid
- customAfter decantation, the solid was triturated with 0.5 mL of ethyl acetate and 0.5 mL of petroleum ether
- filtrationThe solids were filtered
- washwashed with 50% ethyl acetate/petroleum ether
- customdried
- customPurification
- filtrationby filtering an ethyl acetate solution through a layer of silica gel
- customConcentration of the filtrate to 1 mL volume yielded pure crystalline product