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(Diethylamino)sulfur trifluoride → 2-Chloro-5-fluoro-4-(1-fluoro-1-methyl-ethyl)pyrimidine

HRID 521701
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인쇄 미리보기

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HRID 521701 반응식
C(N(S(F)(F)[F:7])CC)C.[Cl:10][C:11]1[N:16]=[C:15]([C:17](O)([CH3:19])[CH3:18])[C:14]([F:21])=[CH:13][N:12]=1>ClCCl>[Cl:10][C:11]1[N:16]=[C:15]([C:17]([F:7])([CH3:19])[CH3:18])[C:14]([F:21])=[CH:13][N:12]=1
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참가 물질

4

반응물 2

HCID 123472(Diethylamino)sulfur trifluorideHCID 866978842-(2-Chloro-5-fluoropyrimidin-4-yl)propan-2-ol

생성물 1

HCID 866978852-Chloro-5-fluoro-4-(1-fluoro-1-methyl-ethyl)pyrimidine수율 87%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
-78 °C

실험 절차

Diethylaminosulfur trifluoride (6.53 g, 40.5 mmol) is added drop wise to a −78° C. solution of 2-(2-chloro-5-fluoro-pyrimidin-4-yl)propan-2-ol (4.825 g, 25.31 mmol) in dichloromethane (70 mL) under nitrogen. The reaction is stirred at −78° C. for 30 minutes under nitrogen, quenched with saturated aqueous sodium bicarbonate, and warmed to room temperature. The reaction mixture is extracted three times with ethyl acetate. The combined organic layers are dried over sodium sulfate and concentrated under vacuum. The resulting crude product is purified using silica gel column chromatography using a 5-100% gradient of ethyl acetate in hexanes to give the title compound (4.23 g, 87%). ES/MS (m/e): 193 and 195 (M+1).

후처리

  1. customquenched with saturated aqueous sodium bicarbonate
  2. temperaturewarmed to room temperature
  3. extractionThe reaction mixture is extracted three times with ethyl acetate
  4. dry with materialThe combined organic layers are dried over sodium sulfate
  5. concentrationconcentrated under vacuum
  6. customThe resulting crude product is purified

출처 및 근거

ORD 기록
ord-bc0fb5ac91984e6c81bb1486ddc59312
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09328124B2

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