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1,3-Dimethylimidazolium Iodide → (2-Fluoro-phenyl)-(2-methylsulfanyl-pyrimidin-4-yl)-methanone

HRID 1946976
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HRID 1946976 반응식
[H-].[Na+].Cl[C:4]1[CH:9]=[CH:8][N:7]=[C:6]([S:10][CH3:11])[N:5]=1.[F:12][C:13]1[CH:20]=[CH:19][CH:18]=[CH:17][C:14]=1[CH:15]=[O:16].[I-].C[N+]1C=CN(C)C=1>O1CCOCC1>[F:12][C:13]1[CH:20]=[CH:19][CH:18]=[CH:17][C:14]=1[C:15]([C:4]1[CH:9]=[CH:8][N:7]=[C:6]([S:10][CH3:11])[N:5]=1)=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 203341,3-Dimethylimidazolium IodideHCID 24758Sodium hydrideHCID 67970o-FluorobenzaldehydeHCID 971134-Chloro-2-methylthiopyrimidine

생성물 1

HCID 59743427(2-Fluoro-phenyl)-(2-methylsulfanyl-pyrimidin-4-yl)-methanone수율 27.2%

시약·촉매·용매 1

HCID 31275
1,4-Dioxane
용매

실험 절차

Sodium hydride (60% dispersion in mineral oil, 598 mg, 14.94 mmol) was added to a stirring solution of 4-chloro-2-methylthiopyrimidine (1.45 mL, 12.45 mmol), 2-fluorobenzaldehyde (1.57 mL, 14.94 mmol) and 1,3-dimethylimidazolium iodide (517 mg, 4.15 mmol) (prepared as described in Org. Synth. (1986) 64:9) in 1,4-dioxane (20 mL). The resulting mixture was heated at reflux for 1 hour; it was then cooled and partitioned between EtOAc and water. The organic layer was separated and dried over Na2SO4, filtered and evaporated under reduced pressure. The crude residue was purified by flash chromatography (hexane/EtOAc, 95/5) to give 840 mg of (2-fluorophenyl)-(2-methylsulfanyl-pyrimidin-4-yl)-methanone.

후처리

  1. temperatureThe resulting mixture was heated
  2. temperatureat reflux for 1 hour
  3. temperatureit was then cooled
  4. custompartitioned between EtOAc and water
  5. customThe organic layer was separated
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. customevaporated under reduced pressure
  9. customThe crude residue was purified by flash chromatography (hexane/EtOAc, 95/5)

출처 및 근거

ORD 기록
ord-99eb2ccdf4e7442fb75b285215c4c38d
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08399462B2

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