Dimethylformamide → 4-Oxo-4-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]-aminobutyric acid

HRID 2240

反応式

HRID 2240 の反応式
N[C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:13][CH2:12][N:11]([C:14]3[CH:19]=[CH:18][N:17]=[CH:16][CH:15]=3)[CH2:10][CH2:9]2)=[CH:4][CH:3]=1.[C:20]1(=[O:26])[O:25][C:23](=[O:24])[CH2:22][CH2:21]1.C[N:28](C=O)C>>[O:26]=[C:20]([C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:13][CH2:12][N:11]([C:14]3[CH:19]=[CH:18][N:17]=[CH:16][CH:15]=3)[CH2:10][CH2:9]2)=[CH:4][CH:3]=1)[CH2:21][CH:22]([NH2:28])[C:23]([OH:25])=[O:24]

参加物

4

反応物 3

HCID 6228DimethylformamideHCID 7922Succinic anhydrideHCID 108904611-(4-Aminophenyl)-4-(4-pyridyl)piperazine

生成物 1

HCID 701103454-Oxo-4-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]-aminobutyric acid

実験手順

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%.

後処理

  1. customa precipitate was collected
  2. washwashed with DMF and ethanol
  3. customdried

出典と根拠

ORDレコード
ord-8d6ceef34f4b4f019e54e9dd2e83cde8
出典データセット
uspto-grants-1998_03
特許番号
US05728701

関連ノート

読み込み中…