Tetrahydrofuran → 1-[1-(2-toluoylmethyl)-2-oxo-5-pivaloyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepin-3-yl]-3-[3-(N,N-dimethylamino)phenyl]urea

HRID 1979320노트

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HRID 1979320 반응식
[C:1](N1C=CN=C1)([N:3]1C=CN=C1)=[O:2].[C:13]1([CH3:41])[C:14]([C:19]([CH2:21][N:22]2[C:28]3[CH:29]=[CH:30][CH:31]=[CH:32][C:27]=3[N:26]([C:33](=[O:38])[C:34]([CH3:37])([CH3:36])[CH3:35])[CH2:25][CH:24]([NH2:39])[C:23]2=[O:40])=[O:20])=[CH:15][CH:16]=[CH:17][CH:18]=1.[CH2:42]([N:44]([CH2:47][CH3:48])[CH2:45]C)C.O1[CH2:53][CH2:52][CH2:51][CH2:50]1>>[C:13]1([CH3:41])[C:14]([C:19]([CH2:21][N:22]2[C:28]3[CH:29]=[CH:30][CH:31]=[CH:32][C:27]=3[N:26]([C:33](=[O:38])[C:34]([CH3:36])([CH3:37])[CH3:35])[CH2:25][CH:24]([NH:39][C:1]([NH:3][C:52]3[CH:51]=[CH:50][CH:48]=[C:47]([N:44]([CH3:42])[CH3:45])[CH:53]=3)=[O:2])[C:23]2=[O:40])=[O:20])=[CH:15][CH:16]=[CH:17][CH:18]=1

참가 물질

5

실험 절차

1,1′-Carbonyldiimidazole (244 mg) was added to a solution of 1-(2-toluoylmethyl)-2-oxo-3-amino-5-pivaloyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine (393 mg) in anhydrous tetrahydrofuran (5 ml), stirred for 30 minutes at room temperature,N,N-dimethyl-m-phenylenediamine dihydrochloride (335 mg) and triethylamine (0.67 ml) was added, and the mixture was refluxed overnight. The reaction mixture was concentrated under reduced pressure, appeared insoluble material was removed and purified by silica gel column chromatography (n-hexane:ethyl acetate=1:1). Etanol was added to the residue for crystallization and filtrated, to thereby obtain 224 mg of the title compound (Yield: 40.3%) as white solid.

후처리

  1. additionwas added
  2. temperaturethe mixture was refluxed overnight
  3. concentrationThe reaction mixture was concentrated under reduced pressure
  4. customwas removed
  5. custompurified by silica gel column chromatography (n-hexane:ethyl acetate=1:1)
  6. additionEtanol was added to the residue for crystallization
  7. filtrationfiltrated

출처 및 근거

ORD 기록
ord-1adb2a6d5a754d88bc4c29a82e6db41b
출처 데이터셋
uspto-grants-2001_05
특허 번호
US06239131B1

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