反应详情

温度

-78 °C

A flask was charged with 3-bromoquinolin-2(1H)-one (U.S. Pat. Appl. Publ. 2002, U.S. 2002099208 A1; Payack, J. F. et al. J. Org. Chem. 2005, 70, 1, 175.) (1.0 g, 4.46 mmol) and sodium hydride (118 mg, 4.91 mmol). The solids were dissolved in tetrahydrofuran (30 mL), stirred for 15 min, and cooled to −78° C. The solution was treated with tert-butyllithium (1.7 M in pentane, 5.25 mL, 8.93 mmol) and stirred for 1 h. To this was added N-tert-butoxycarbonyl-4-piperidone (889 mg, 1.0 equiv). The ice bath was removed and stirring continued for 1 h. The reaction was quenched by addition of saturated ammonium chloride. The reaction was diluted with diethyl ether, washed with water (2×), then brine, dried over magnesium sulfate, and concentrated. The resulting oil was triturated with diethyl ether to give a white solid which was filtered, washed with diethyl ether, and air dried to give 430 mg (28%) as a white powder. 1H-NMR (CDCl3, 500 MHz) δ 1.48 (s, 9H), 1.57 (bs, 2H), 1.87 (m, 2H), 2.13 (m, 2H), 3.37 (m, 2H), 4.06 (m, 2H), 7.28 (m, 2H), 7.53 (m, 2H), 7.60 (m, 1H), 7.69 (s, 1H). Mass spec.: 367.35 (MNa)+.

1. stirringstirred for 1 h
2. customThe ice bath was removed
3. stirringstirring
4. waitcontinued for 1 h
5. customThe reaction was quenched by addition of saturated ammonium chloride
6. additionThe reaction was diluted with diethyl ether
7. washwashed with water (2×)
8. dry with materialbrine, dried over magnesium sulfate
9. concentrationconcentrated
10. customThe resulting oil was triturated with diethyl ether
11. customto give a white solid which
12. filtrationwas filtered
13. washwashed with diethyl ether, and air
14. customdried
15. customto give 430 mg (28%) as a white powder