3-Amino-4-bromo-N-(2-(4-methylpiperazin-1-yl)benzyl)benzamide → N-(2-Bromo-5-(2-(4-methylpiperazin-1-yl)benzylcarbamoyl)phenyl)imidazo[1,2-a]pyridine-3-carboxamide
反応式
Cl.[N:2]1[CH:3]=[C:4]([C:11](Cl)=[O:12])[N:5]2[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=12.[NH2:14][C:15]1[CH:16]=[C:17]([CH:35]=[CH:36][C:37]=1[Br:38])[C:18]([NH:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=1[N:28]1[CH2:33][CH2:32][N:31]([CH3:34])[CH2:30][CH2:29]1)=[O:19]>N1C=CC=CC=1>[Br:38][C:37]1[CH:36]=[CH:35][C:17]([C:18](=[O:19])[NH:20][CH2:21][C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=2[N:28]2[CH2:29][CH2:30][N:31]([CH3:34])[CH2:32][CH2:33]2)=[CH:16][C:15]=1[NH:14][C:11]([C:4]1[N:5]2[CH:10]=[CH:9][CH:8]=[CH:7][C:6]2=[N:2][CH:3]=1)=[O:12]参加物
4
実験手順
Imidazo[1,2-a]pyridine-3-carbonyl chloride hydrochloride (0.97 mg, 4.46 mmol) was slowly added in portions to a stirred solution of 3-amino-4-bromo-N-(2-(4-methylpiperazin-1-yl)benzyl)benzamide (step 1) (900 mg, 2.23 mmol) in dry pyridine (15 ml). The reaction was stirred at RT for 18 hrs and quenched with water. The solvent removed in vacuo. The residue was treated with a small amount of MeOH to dissolve insoluble material then partitioned between aq. NaHCO3 and DCM. The organic extract was washed with brine, dried over MgSO4 and concentrated in vacuo. The crude product mixture was crystallised from MeOH to give a white solid;
後処理
- customquenched with water
- customThe solvent removed in vacuo
- additionThe residue was treated with a small amount of MeOH
- dissolutionto dissolve insoluble material
- customthen partitioned between aq. NaHCO3 and DCM
- extractionThe organic extract
- washwas washed with brine
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo
- customThe crude product mixture was crystallised from MeOH
- customto give a white solid
出典と根拠
- ORDレコード
- ord-965d7e547a7d4df493836fa1aca07ca9
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08883819B2
反応ノート
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