反应详情

A mixture of 6-benzyloxy-1-[4-(2-pyrrolidin-1-yl-ethoxy)phenyl]-1,2,3,4-tetrahydroisoquinoline (0.300 g, 0.70 mmol), ammonium formate (0.883 g, 14.0 mmol), and 20% Pd(OH)2/C (0.050 g) in MeOH (50 ml) was refluxed under N2 for 1 hr, then filtered through Celite®. The filtrate was evaporated in vacuo to a yellow residue that was suspended in a mixture of H2O (5 ml) and saturated NaHCO3 solution (5 ml), then extracted with CH2Cl2 (4×10 ml). The combined organic extracts were dried over MgSO4 and concentrated in vacuo to give 0.133 g of yellow oil. The aqueous layer was extracted again with CH2Cl2 (4×50 ml) to give an additional 0.083 g of yellow oil, for a total of 0.216 g (91% yield) of product.

1. temperaturewas refluxed under N2 for 1 hr
2. filtrationfiltered through Celite®
3. customThe filtrate was evaporated in vacuo to a yellow residue that
4. additionwas suspended in a mixture of H2O (5 ml) and saturated NaHCO3 solution (5 ml)
5. extractionextracted with CH2Cl2 (4×10 ml)
6. dry with materialThe combined organic extracts were dried over MgSO4
7. concentrationconcentrated in vacuo