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Methyl iodide → benzyl 8-bromo-1,5-dimethyl-2-oxo-2,3-dihydro-1H-1,4-benzodiazepin-3-ylcarbamate

HRID 1061536
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HRID 1061536 반응식
[Br:1][C:2]1[CH:25]=[CH:24][C:5]2[C:6]([CH3:23])=[N:7][CH:8]([NH:12][C:13](=[O:22])[O:14][CH2:15][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)[C:9](=[O:11])[NH:10][C:4]=2[CH:3]=1.[C:26](=O)([O-])[O-].[K+].[K+].IC>CN(C)C=O.O.C(OCC)(=O)C>[Br:1][C:2]1[CH:25]=[CH:24][C:5]2[C:6]([CH3:23])=[N:7][CH:8]([NH:12][C:13](=[O:22])[O:14][CH2:15][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)[C:9](=[O:11])[N:10]([CH3:26])[C:4]=2[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 135850842HCID 135850842, 화합물

생성물 1

HCID 21941566benzyl 8-bromo-1,5-dimethyl-2-oxo-2,3-dihydro-1H-1,4-benzodiazepin-3-ylcarbamate수율 77.5%

시약·촉매·용매 3

HCID 962Water용매HCID 6228
Dimethylformamide
용매
HCID 8857Ethyl Acetate용매

실험 절차

162b (2.0 g, 4.98 mmol) was dissolved in anhydrous N,N-dimethylformamide (10 ml), to this was added potassium carbonate (1.72 g, 12.44 mmol) and iodomethane (0.847 g, 5.97 mmol) and the reaction was sealed in a pressure flask and stirred for 12 hours at room temperature. The reaction was diluted with water and ethyl acetate (20/70 ml). The aqueous solution was then extracted with ethyl acetate (3×20 ml). The organic layers combined, washed with water (1×100 ml), dried over magnesium sulfate, filtered and the filtrate concentrated to give the title compound 162c (1.58 g, 77.5%). 1H NMR (CDCl3, 300 MHz): δ 7.43-7.28 (m, 7H), 6.68 (d, 1H, J=8.1 Hz), 5.15-5.05 (m, 3H), 3.38 (s, 3H), 2.45 (d, 3H, 1.5 Hz) ppm.

후처리

  1. customthe reaction was sealed in a pressure flask
  2. extractionThe aqueous solution was then extracted with ethyl acetate (3×20 ml)
  3. washwashed with water (1×100 ml)
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationthe filtrate concentrated

출처 및 근거

ORD 기록
ord-430568507ec54884b42858af4866ff25
출처 데이터셋
uspto-grants-2005_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06960576B2

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