Iodine → 2-Chloro-5-fluoro-4-isopropyl-pyrimidine

HRID 338063노트

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HRID 338063 반응식
[F:1][C:2]1[CH:3]=[N:4][C:5]([Cl:8])=[N:6][CH:7]=1.[CH:9]([Mg]Cl)([CH3:11])[CH3:10].C(N(CC)CC)C.II>COCCOC.O1CCCC1>[Cl:8][C:5]1[N:6]=[C:7]([CH:9]([CH3:11])[CH3:10])[C:2]([F:1])=[CH:3][N:4]=1

참가 물질

7

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온도
0 °C

실험 절차

A solution of 5-fluoro-2-chloropyrimidine (5.00 g, 37.7 mmol) in 1,2-dimethoxyethane (25 mL) is treated with a solution of 2 M isopropyl magnesium chloride in tetrahydrofuran (28.3 mL, 56.6 mmol) while keeping the temperature below 15° C. The resulting solution is stirred for one hour under nitrogen and then cooled to 0° C. and treated drop wise with a solution of triethylamine (5.76 mL, 37.7 mmol) in tetrahydrofuran (5 mL). A solution of iodine (9.58 g, 37.7 mmol) in tetrahydrofuran (20 mL) is added. The reaction is quenched with water and saturated sodium bicarbonate and saturated sodium bisulfate are added. The mixture is extracted three times with ethyl acetate. The combined organic layers are dried over sodium sulfate and the solvent is removed under vacuum. The crude product is purified over silica gel with a 30 minute gradient, dichloromethane/hexanes (5 to 100%) to give the title compound (2.55 g, 39%). GC/MS (m/e): 174.

후처리

  1. customthe temperature below 15° C
  2. customThe reaction is quenched with water and saturated sodium bicarbonate and saturated sodium bisulfate
  3. additionare added
  4. extractionThe mixture is extracted three times with ethyl acetate
  5. dry with materialThe combined organic layers are dried over sodium sulfate
  6. customthe solvent is removed under vacuum
  7. customThe crude product is purified over silica gel with a 30 minute gradient, dichloromethane/hexanes (5 to 100%)

출처 및 근거

ORD 기록
ord-fb74de0fbbbd48fc942790f823784b9e
출처 데이터셋
uspto-grants-2014_11
특허 번호
US08889856B2

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