反应详情

温度

80 °C

Prepared by Procedure H and Scheme S. A mixture of N-(3-{1-[4-(1,3-dioxolan-2-yl)butyl]-4-piperidinyl}phenyl)-2-methylpropanamide (100 mg, 0.270 mmol), 1-methyl-1-phenylhydrazine (106 mg, 0.870 mmol), ZnCl2 (119 mg, 0.870 mmol) and HOAc (1.00 mL) was heated for 12 h at 80° C. The resulting crude mixture was diluted with water (20 mL), the aqueous layer was neutralized with a saturated K2CO3 solution (10 mL) and extracted with CH2Cl2 (3×20 mL). The combined organic layers were concentrated in vacuo and the residue was purified by preparative TLC using 3% of NH3 (2.0 M in methanol) in CH2Cl2 to give the desired product 2-methyl-N-(3-{1-[3-(1-methyl-1H-indol-3-yl)propyl]-4-piperidinyl}phenyl)propanamide (20.7 mg, 18.7%): 1H NMR (400 MHz, CDCl3) δ 7.60 (d, 1H, J=8.1 Hz), 7.45 (s, 1H), 7.35 (d, 1H, J=7.4 Hz), 7.25 (m, 4H), 7.09 (t, 1H, J=7.3 Hz), 6.97 (d, 1H, J=7.3 Hz), 6.86 (s, 1H), 3.75 (s, 3H), 3.11 (d, 2H, J=11.6 Hz), 2.79 (t, 2H, J=7.3 Hz), 2.51 (m, 4H), 2.12-1.81 (m, 8H), 1.25 (d, 6H, J=7.1 Hz); Anal. Calcd for C27H35N3O+0.225 CHCl3: C, 73.57; H, 7.99; N, 9.45. Found: C, 73.93; H, 7.90; N, 9.23; ESMS m/e: 418.2 (M+H)+.

1. customPrepared by Procedure H and Scheme S
2. extractionextracted with CH2Cl2 (3×20 mL)
3. concentrationThe combined organic layers were concentrated in vacuo
4. customthe residue was purified by preparative TLC