反应详情

A solution of 2-[2-(3,5-Bis-trifluoromethyl-phenyl)-6-(4-trifluoromethyl-phenyl)-pyridin-4-yl]-4-methyl-pent-4-enoic acid methyl ester (80 mg, 0.14 mmol), Pd/C (10%, 10 mg) in methanol (10 mL) was hydrogenated for 4 h. The mixture was filtered through Celite, washed with methanol, evaporated. The residue was dissolved in CH2Cl2, filtered and evaporated to give the product as a colorless oil (80 mg, 100%). 1H NMR (300 MHz, CDCl3) δ 8.56 (s, 2H), 8.24 (d, J=7.91 Hz, 2H), 7.96 (s, 1H), 7.70-7.85 (m, 4H), 3.80-3.92 (m, 1H), 3.73 (s, 3H), 2.14 (ddd, J=6.97, 8.48, 13.56 Hz, 1H), 1.76 (dt, J=7.06, 13.75 Hz, 1H), 1.50-1.65 (m, 1H), 0.98 (d, J=6.78 Hz, 6H). MS m/e 564.2 (M+H).

1. filtrationThe mixture was filtered through Celite
2. washwashed with methanol
3. customevaporated
4. dissolutionThe residue was dissolved in CH2Cl2
5. filtrationfiltered
6. customevaporated