反应详情

4-[4-Amino-4-(4-chlorobenzyl)-piperidin-1-yl]-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid ethyl ester (55 mg, 0.13 mmol) was suspended in 2M potassium hydroxide (1.5 mL) and irradiated in a microwave reactor (250 W) for 2 hours at 120° C. After cooling, water (2 mL) was added and the solids formed were collected by filtration. The filtrate was extracted with ethyl acetate (2×4 mL) and dried (Na2SO4). The extracts were evaporated and the resulting yellow solids were combined with the previous material and dissolved in acetone (10 mL) and n-hexanes (2 mL). The solvents were concentrated until precipitation occurred. The solids were collected by filtration and washed with n-hexanes to give 4-(4-chlorobenzyl)-1-(1H-pyrazolo[3,4-b]pyridin-4-yl)-piperidin-4-ylamine as a light yellow powder (26 mg, 57%). LC-MS (LCT2) m/z 342 [M+H+], Rt 2.07 min.

1. customirradiated in a microwave reactor (250 W) for 2 hours at 120° C
2. temperatureAfter cooling
3. customthe solids formed
4. filtrationwere collected by filtration
5. extractionThe filtrate was extracted with ethyl acetate (2×4 mL)
6. dry with materialdried (Na2SO4)
7. customThe extracts were evaporated
8. dissolutiondissolved in acetone (10 mL)
9. concentrationThe solvents were concentrated until precipitation
10. filtrationThe solids were collected by filtration
11. washwashed with n-hexanes