反应详情

To a solution of 5-bromo-1-methyl-1H-imidazole (1.14 g, 7.11 mmol) in DCM was added ethyl magnesium bromide (2.34 mL, 7.11 mmol; 3.0 M in diethyl ether) dropwise over a 10 minute period. The resulting pale yellow solution was stirred at room temperature for 15 minutes, cooled in an ice bath to 0° C. and N-methoxy-N-methylthiazole-5-carboxamide (1.02 g, 5.92 mmol, Intermediate 11: step a) dissolved in DCM (3 mL) was added dropwise. The cold bath was removed and the reaction mixture stirred at room temperature for 48 hours. To the resulting yellow suspension was added water followed by 6 M aqueous HCl to a neutral pH (pH=6-7). The aqueous mixture was extracted with DCM, dried over Na2SO4, filtered and concentrated. Et2O was added and the mixture sonicated. The precipitate was collected by filtration and dried to provide the title compound as a tan solid.

1. temperaturecooled in an ice bath to 0° C.
2. additionwas added dropwise
3. customThe cold bath was removed
4. stirringthe reaction mixture stirred at room temperature for 48 hours
5. additionTo the resulting yellow suspension was added water
6. extractionThe aqueous mixture was extracted with DCM
7. dry with materialdried over Na2SO4
8. filtrationfiltered
9. concentrationconcentrated
10. additionEt2O was added
11. customthe mixture sonicated
12. filtrationThe precipitate was collected by filtration
13. customdried