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

HRID 335284노트

반응식

HRID 335284 반응식
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]

참가 물질

4

실험 절차

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;

후처리

  1. customquenched with water
  2. customThe solvent removed in vacuo
  3. additionThe residue was treated with a small amount of MeOH
  4. dissolutionto dissolve insoluble material
  5. customthen partitioned between aq. NaHCO3 and DCM
  6. extractionThe organic extract
  7. washwas washed with brine
  8. dry with materialdried over MgSO4
  9. concentrationconcentrated in vacuo
  10. customThe crude product mixture was crystallised from MeOH
  11. customto give a white solid

출처 및 근거

ORD 기록
ord-965d7e547a7d4df493836fa1aca07ca9
출처 데이터셋
uspto-grants-2014_11
특허 번호
US08883819B2

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