Benzyl Chloride → HCID 797337, 화합물

HRID 1471218

반응식

HRID 1471218 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[NH:8][C:9]2[CH:15]=[CH:14][CH:13]=[CH:12][C:10]=2[N:11]=1.C(=O)([O-])[O-].[K+].[K+].[CH2:22](Cl)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>CN(C)C=O>[CH2:22]([N:11]1[C:10]2[CH:12]=[CH:13][CH:14]=[CH:15][C:9]=2[N:8]=[C:7]1[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][N:1]=1)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1

참가 물질

5

반응물 3

HCID 7503Benzyl Chloride2회HCID 11430Potassium CarbonateHCID 708212-(2'-Pyridyl)benzimidazole

생성물 1

HCID 797337HCID 797337, 화합물수율 82.1%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a flask were added 2.0 g 2-(2-pyridyl)benzimidazole, 1.8 g potassium carbonate, 30 ml N,N-dimethylformamide and the mixture was stirred under nitrogen at 10 C. 1.5 g benzyl chloride were added and the mixture allowed to warm to 22 C and stirred for 3 hours. Another 0.3 g benzyl chloride was added and the reaction was stirred at 22 C for another 16 hours. The reaction was quenched with 40 ml water and the product was filtered and washed with water. The product was dissolved in 10 ml ethanol and 15 ml of water were added. After cooling to 5 C, the product was filtered, washed and dried resulting in 2.4 g of off-white solid.

후처리

  1. temperatureto warm to 22 C
  2. stirringstirred for 3 hours
  3. stirringthe reaction was stirred at 22 C for another 16 hours
  4. customThe reaction was quenched with 40 ml water
  5. filtrationthe product was filtered
  6. washwashed with water
  7. dissolutionThe product was dissolved in 10 ml ethanol
  8. addition15 ml of water were added
  9. temperatureAfter cooling to 5 C
  10. filtrationthe product was filtered
  11. washwashed
  12. customdried

출처 및 근거

ORD 기록
ord-14e8acd89480434399c4e2728ae66fb3
출처 데이터셋
uspto-grants-2015_04
특허 번호
US09011734B2

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