反应 #2336

ord-8d6ceef34f4b4f019e54e9dd2e83cde8

反应方程式

Nc1ccc(N2CCN(c3ccncc3)CC2)cc1
1-(4-aminophenyl)-4-(4-pyridyl)piperazine
O=C1CCC(=O)O1
succinic anhydride
CN(C)C=O
DMF
NC(CC(=O)c1ccc(N2CCN(c3ccncc3)CC2)cc1)C(=O)O
title compound
NC(CC(=O)c1ccc(N2CCN(c3ccncc3)CC2)cc1)C(=O)O
4-oxo-4-[4-[4-(4-pyridyl)piperazin-1-yl]-phenyl]-aminobutyric acid

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他a precipitate was collected
  2. 2
    洗涤washed with DMF and ethanol
  3. 3
    其他dried

实验过程

To a solution of 1-(4-aminophenyl)-4-(4-pyridyl)piperazine (100 mg) in DMF (8 ml) was added succinic anhydride (79 mg). The reaction mixture was stirred at room temperature for 2.5 hr and a precipitate was collected, washed with DMF and ethanol, then dried to give the title compound (106 mg) as a beige-coloured solid: m.p. 263°-264° C.; NMR (d6 -DMSO+CF3CO2H) δ 2.68 (4H, m), 3.80 (4H, m), 4.19 (4H, m), 7.20 (2H, d), 7.56 (2H, d), 7.82 (2H, d), 8.21 (2H, d), 9.62 (1H, s); m/Z 355 (M+H)+ ; calculated for C19H22N4 O3. 0.4 H2O: C, 63.1%; H, 6.36%; N, 15.5%; found: C, 63.1%; H, 6.4%; N, 15.7%.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05728701uspto-grants-1998_03