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Methyl iodide → 5-(3,5-dimethylphenylthio)-4-isopropyl-1-methyl-1H-imidazole

HRID 1857689
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HRID 1857689 반응식
[CH3:1][C:2]1[CH:3]=[C:4]([S:9][C:10]2[NH:14][CH:13]=[N:12][C:11]=2[CH:15]([CH3:17])[CH3:16])[CH:5]=[C:6]([CH3:8])[CH:7]=1.[H-].[Na+].[CH3:20]I>CN(C)C=O>[CH3:1][C:2]1[CH:3]=[C:4]([S:9][C:10]2[N:14]([CH3:20])[CH:13]=[N:12][C:11]=2[CH:15]([CH3:17])[CH3:16])[CH:5]=[C:6]([CH3:8])[CH:7]=1
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 1784253375-(3,5-dimethylphenylthio)-4-isopropyl-1H-imidazole

생성물 1

HCID 221301155-(3,5-dimethylphenylthio)-4-isopropyl-1-methyl-1H-imidazole수율 79%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

In 10 ml of dry N,N-dimethylformamide was dissolved 1.0 g (4.1 mmol) of 5-(3,5-dimethylphenylthio)-4-isopropyl-1H-imidazole (X=Y=Me) (9), followed by addition of 330 mg (8.3 mmol) of 60% sodium hydride under ice-cooling. After 5 minutes, 690 mg (4.9 mmol) of methyl iodide was added and the mixture was stirred for 10 minutes. This reaction mixture was poured in ice-water and extracted with diethyl ether. The organic layer was washed with water and dried over sodium sulfate. The solvent was then distilled off under reduced pressure and the residue was fractionated by alumina chromatography (ethyl acetate:n-hexane=1:1). From the first fraction, 833 mg (yield 79%) of 5-(3,5-dimethylphenylthio)-4-isopropyl-1-methyl-1H-imidazole (X=Y=Me) (10) was recovered as oil.

후처리

  1. temperaturecooling
  2. extractionextracted with diethyl ether
  3. washThe organic layer was washed with water
  4. dry with materialdried over sodium sulfate
  5. distillationThe solvent was then distilled off under reduced pressure

출처 및 근거

ORD 기록
ord-3198974dafb34fa58f7a1bd66f386256
출처 데이터셋
uspto-grants-2000_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06147097

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