Thionyl Chloride → 1h-Benzimidazole,6-(chloromethyl)-1-[(2-chlorophenyl)methyl]-2-methyl-,hydrochloride

HRID 276036노트

반응식

HRID 276036 반응식
S(Cl)([Cl:3])=O.[Cl:5][C:6]1[CH:24]=[CH:23][CH:22]=[CH:21][C:7]=1[CH2:8][N:9]1[C:13]2[CH:14]=[C:15]([CH2:18]O)[CH:16]=[CH:17][C:12]=2[N:11]=[C:10]1[CH3:20]>>[ClH:3].[Cl:5][C:6]1[CH:24]=[CH:23][CH:22]=[CH:21][C:7]=1[CH2:8][N:9]1[C:13]2[CH:14]=[C:15]([CH2:18][Cl:3])[CH:16]=[CH:17][C:12]=2[N:11]=[C:10]1[CH3:20]

참가 물질

3

반응물 2

HCID 24386Thionyl ChlorideHCID 183155381h-Benzimidazole-6-methanol,1-[(2-chlorophenyl)methyl]-2-methyl-

생성물 1

HCID 226203411h-Benzimidazole,6-(chloromethyl)-1-[(2-chlorophenyl)methyl]-2-methyl-,hydrochloride

실험 절차

Five milliliters of thionyl chloride were added to 3.56 g of 1-(2-chlorobenzyl)-6-hydroxymethyl-2-methylbenzimidazole, and the mixture was stirred at room temperature for 20 minutes and then at 80° C. for 20 minutes. After excess thionyl chloride was distilled off under reduced pressure, the residue was dissolved in 10 ml of chloroform, and the solution was crystallized from hexane. The crystals were separated through filtration, washed with hexane, and dried to give 4.07 g of 1-(2-chlorobenzyl)-6-chloromethyl-2-methylbenzimidazole hydrochloride.

후처리

  1. waitat 80° C. for 20 minutes
  2. distillationAfter excess thionyl chloride was distilled off under reduced pressure
  3. dissolutionthe residue was dissolved in 10 ml of chloroform
  4. customthe solution was crystallized from hexane
  5. customThe crystals were separated through filtration
  6. washwashed with hexane
  7. customdried

출처 및 근거

ORD 기록
ord-5b8139e6faba4baba6797863d10ed5c4
출처 데이터셋
uspto-grants-2002_03
특허 번호
US06352985B1

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