反应详情

To a solution of 5-cyano-2-{[(2-nitro-benzenesulfonyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amino}-methyl}-benzoic acid methyl ester (2.32 g, 5.72 mmol) dissolved in THF (50 mL) and MeOH (50 mL), LiBH4 (1.26 g, 57.2 mmol) was slowly added. The mixture was stirred at room temperature under a positive pressure of N2 for 2 hours. The mixture was concentrated in vacuo and redissolved in CH2Cl2 (50 mL). Brine (30 mL) was added and the resulting mixture was extracted with CH2Cl2 (2×50 mL). The combined organic extracts were dried (Na2SO4), filtered, and concentrated in vacuo to afford a yellow solid. Purification via column chromatography on silica gel (hexanes:EtOAc, 1:1, v/v) afforded N-(4-cyano-2-hydroxymethyl-benzyl)-2-nitro-N-(5,6,7,8-tetrahydro-quinolin-8-yl)-benzenesulfonamide as a yellow solid (2.32 g, 85%). 1H NMR (CDCl3) δ 1.56 (s, 9H), 1.91 (m, 2H), 2.36 (m, 1H), 2.61 (m, 2H), 2.98 (m, 1H), 4.23 (d, 1H, J=16.7 Hz), 4.61 (m, 2H), 4.90 (d, 1H, J=16.2 Hz), 5.21 (m, 1H), 7.03 (dd, 1H, J=5.3, 9.7 Hz), 7.37 (m, 3H), 7.67 (m, 4H), 7.95 (d, 1H, J=7.9 Hz), 8.16 (d, 1H, J=4.4 Hz).

1. concentrationThe mixture was concentrated in vacuo
2. dissolutionredissolved in CH2Cl2 (50 mL)
3. additionBrine (30 mL) was added
4. extractionthe resulting mixture was extracted with CH2Cl2 (2×50 mL)
5. dry with materialThe combined organic extracts were dried (Na2SO4)
6. filtrationfiltered
7. concentrationconcentrated in vacuo
8. customto afford a yellow solid
9. customPurification via column chromatography on silica gel (hexanes