反应详情

A round-bottom flask was charged with 1-(4-fluoro-2-hydroxy-5-nitrophenyl)-4-methyl-1H-tetrazol-5(4H)-one (500 mg, 1.96 mmol), EtOH (20 mL), HOAc (250 uL), and 10% Pd/C (50% in water, Degussa type E101; 100 mg, 20 wt % by weight of the starting nitro compound). The flask was sealed with a rubber septum, degassed, and back-filled with H2 (×3) from a balloon filled with H2. The reaction was stirred for 2 h using a H2 filled balloon. The reaction mixture was filtered through a pad of celite, and the pad of celite was rinsed with MeOH. The filtrate was evaporated to dryness, and the product dried in vacuo with a water bath at 45° C. to remove any residual HOAc to provide 1-(5-amino-4-fluoro-2-hydroxyphenyl)-4-methyl-1H-tetrazol-5(4H)-one (437 mg, 99%) as a brown solid that was used without further purification. 1H NMR (300 MHz; d6-DMSO) δ 9.46 (s, 1H), 6.67-6.72 (m, 2H), 4.80 (bs, 2H), 3.56 (s, 3H); 19F NMR (282 MHz; d6-DMSO) δ −128.6 (t); m/z=225 (M+H)+.

1. customThe flask was sealed with a rubber septum
2. customdegassed
3. additionback-filled with H2 (×3) from a balloon
4. additionfilled with H2
5. filtrationThe reaction mixture was filtered through a pad of celite
6. washthe pad of celite was rinsed with MeOH
7. customThe filtrate was evaporated to dryness
8. customthe product dried in vacuo with a water bath at 45° C.
9. customto remove any residual HOAc