反应详情

720 mg ethyl 8-[(2,6-difluorobenzyl)oxy]-2-methyl-6-[(trimethylsilyl)ethynyl]imidazo[1,2-a]-pyridine-3-carboxylate (Example 37A; 1.63 mmol; 1 equivalent) were initially charged in 16 ml of methanol, and 674 mg of potassium carbonate (4.81 mmol, 3 equivalents) were added. The resulting reaction mixture was stirred at room temperature for 2 h. The reaction mixture was then concentrated, water was added and the mixture was extracted three times with ethyl acetate. The combined organic phases were washed with saturated sodium chloride solution and dried over magnesium sulphate, and the filtrate was concentrated. This gave 587.7 mg of crude product (which contained 35% of the methyl ester of the target compound; quantitative yield) which was used without further purification for the next reaction.

1. customThe resulting reaction mixture
2. concentrationThe reaction mixture was then concentrated
3. additionwater was added
4. extractionthe mixture was extracted three times with ethyl acetate
5. washThe combined organic phases were washed with saturated sodium chloride solution
6. dry with materialdried over magnesium sulphate
7. concentrationthe filtrate was concentrated
8. customquantitative yield) which was used without further purification for the next reaction