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Methyl iodide → 4-(2,6-Dimethyl-4-fluorobenzylamino)-2,2-dimethylbenzimidazole

HRID 991596
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HRID 991596 반응식
[CH3:1][C:2]1[CH:19]=[C:18]([F:20])[CH:17]=[C:16]([CH3:21])[C:3]=1[CH2:4][NH:5][C:6]1[C:14]2[NH:13][C:12]([CH3:15])=[N:11][C:10]=2[CH:9]=[CH:8][CH:7]=1.[OH-].[Na+].[CH3:24]I>COCCOC.[Br-].C([N+](CCCC)(CCCC)CCCC)CCC>[CH3:1][C:2]1[CH:19]=[C:18]([F:20])[CH:17]=[C:16]([CH3:21])[C:3]=1[CH2:4][NH:5][C:6]1[C:14]2[C:10](=[N:11][C:12]([CH3:24])([CH3:15])[N:13]=2)[CH:9]=[CH:8][CH:7]=1
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참가 물질

6

반응물 3

HCID 6328Methyl iodideHCID 14798Sodium HydroxideHCID 178432169HCID 178432169, 화합물

생성물 1

HCID 867585704-(2,6-Dimethyl-4-fluorobenzylamino)-2,2-dimethylbenzimidazole수율 76.9%

시약·촉매·용매 2

HCID 74236Tetrabutylammonium Bromide촉매HCID 8071
1,2-Dimethoxyethane
용매

실험 절차

4-(2,6-Dimethyl-4-fluorobenzylamino)-2-methylbenzimidazole (0.1 g, 0.35 mmol) was dissolved in 1,2-dimethoxyethane (3 ml). Solid sodium hydroxide (25 mg, 0.63 mmol) and tetrabutylammonium bromide (5 mg, 0.016 mmol) were added. The mixture was stirred 15 minutes at ambient temperature. Methyl iodide (60 mg 0.42 mmol) was added and the reaction mixture was stirred at ambient temperature for 2.5 h. The solvent was evaporated under reduced pressure. The residue was purified by column chromatography on silica gel, using methylene chloride: ethyl acetate (50: 50) as eluent. 80 mg (76%) of the title compound was obtained.

후처리

  1. stirringthe reaction mixture was stirred at ambient temperature for 2.5 h
  2. customThe solvent was evaporated under reduced pressure
  3. customThe residue was purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-31147a9adb5e4e65967c3cea1f444ef4
출처 데이터셋
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06465505B1

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