反应详情

To a solution of racemic-1-(2-fluoro-4-nitrophenyl)-trans-2,4,5-trimethylpiperazine (0.10 g, 0.4 mmol) in 4 mL EtOH is added 0.04 g of 5% Pd/C. The atmosphere over the reaction is evacuated and replaced with H2 thrice and then fitted with a balloon filled with H2 gas. After stirring 12 h, the crude reaction mixture is filtered through Celite, rinsed with EtOH, concentrated in vacuo and chromatographed (silica gel, 10% MeOH in CH2Cl2) to give 0.027 g (0.12 mmol, 32%) of racemic-3-fluoro-4-(trans-2,4,5-trimethylpiperazin-1-yl)aniline as a yellow liquid. 1H NMR (300 MHz, CDCl3) δ 0.86 (d, J=6.0 Hz, 3H), 1.07 (d, J=6.0 Hz, 3H), 2.16 (t, J=10.8 Hz, 2H), 2.34 (s, 3H), 2.72 (t, 1H), 2.83-2.92 (m, 2H), 3.19 (br. s., 1H), 3.58 (br. s., 2H), 6.32-6.40 (m, 2H), 6.92-7.00 (m, 1H). LCMS-ESI (m/z): calcd for C13H20FN3, 237.1; [M+H]+ found, 238.2.

1. customThe atmosphere over the reaction is evacuated
2. customfitted with a balloon
3. additionfilled with H2 gas
4. customthe crude reaction mixture
5. filtrationis filtered through Celite
6. washrinsed with EtOH
7. concentrationconcentrated in vacuo
8. customchromatographed (silica gel, 10% MeOH in CH2Cl2)