5-Bromo-1-methyl-1H-imidazole → (1-Methyl-1H-imidazol-5-yl)(4-nitrophenyl)methanone

HRID 526838

반응식

HRID 526838 반응식
Br[C:2]1[N:6]([CH3:7])[CH:5]=[N:4][CH:3]=1.C([Mg]Br)C.CON(C)[C:15](=[O:25])[C:16]1[CH:21]=[CH:20][C:19]([N+:22]([O-:24])=[O:23])=[CH:18][CH:17]=1>C(Cl)Cl>[CH3:7][N:6]1[C:2]([C:15]([C:16]2[CH:17]=[CH:18][C:19]([N+:22]([O-:24])=[O:23])=[CH:20][CH:21]=2)=[O:25])=[CH:3][N:4]=[CH:5]1

참가 물질

5

실험 절차

To a solution of 5-bromo-1-methyl-1H-imidazole (3.22 g, 19.98 mmol) in DCM (15 mL) was added ethyl magnesium bromide (6.66 mL, 19.98 mmol, 3.0 M in diethyl ether) dropwise over a 10 minute period. The resulting orange-red solution was stirred at room temperature for 15 minutes, cooled in an ice bath to 0° C. and N-methoxy-N-methyl-4-nitrobenzamide (3.5 g, 16.65 mmol, Intermediate 7: step a) dissolved in DCM (10 mL) was added dropwise. The ice bath was removed and the solid suspension stirred at room temperature for 48 hours. Water was added followed by 6 M aqueous HCl to a neutral pH (pH=6-7). The aqueous mixture was extracted with DCM, dried over Na2SO4, filtered and concentrated. Et2O was added and the mixture sonicated. The precipitate was collected by filtration and dried to provide the title compound as a tan solid.

후처리

  1. temperaturecooled in an ice bath to 0° C.
  2. additionwas added dropwise
  3. customThe ice bath was removed
  4. stirringthe solid suspension stirred at room temperature for 48 hours
  5. additionWater was added
  6. extractionThe aqueous mixture was extracted with DCM
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated
  10. additionEt2O was added
  11. customthe mixture sonicated
  12. filtrationThe precipitate was collected by filtration
  13. customdried

출처 및 근거

ORD 기록
ord-b41eba38d3cc48979088abf09e668c45
출처 데이터셋
uspto-grants-2016_05
특허 번호
US09346782B2

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