反应 #3294
ord-7c0d2f4521364c5dbc8d4b38d2935639
反应方程式
反应物
试剂
无
反应条件
温度
180°CELSIUS
详细条件
See reaction.notes.procedure_details.
后处理
- 1温度was heated
- 2温度The resulting solution was heated for 10 minutes
- 3其他Much of the excess 4-methylaniline was evaporated at reduced pressure
- 4workup.DISSOLUTIONThe remainder was dissolved in 1 mL of ethyl acetate
- 5其他The crystals that separated from the dark solution
- 6过滤were filtered
- 7洗涤washed with 2 mL of ethyl acetate
- 8其他Recrystallization from ethyl acetate
- 9其他gave pure product
实验过程
A mixture of 0.113 g (0.29 mmol) of 6-(2,6-dichlorophenyl)-2-methanesulfonyl-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one of Example 39 and 0.50 g (4.70 mmol) of 4-methylaniline was heated, with stirring, in a 180° C. oil bath. The resulting solution was heated for 10 minutes. Much of the excess 4-methylaniline was evaporated at reduced pressure. The remainder was dissolved in 1 mL of ethyl acetate. The crystals that separated from the dark solution were filtered and washed with 2 mL of ethyl acetate and then ether; wt 0.111 g. Recrystallization from ethyl acetate gave pure product; wt 0.050 g; mp 243°-245° C.