홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

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

HRID 1415985
노트
인쇄 미리보기

반응식

HRID 1415985 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
참가 물질실험 절차후처리출처 및 근거반응 노트

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-0185f45252164bb2a8dfede20075943b
출처 데이터셋
uspto-grants-1999_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05910506

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트