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Imidazole → Pyrimidine, 2-(1,1-difluoro-2-iodoethyl)-

HRID 1171070
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HRID 1171070 반응식
[F:1][C:2]([F:11])([C:5]1[N:10]=[CH:9][CH:8]=[CH:7][N:6]=1)[CH2:3]O.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.N1C=CN=C1.[I:36]I>C1(C)C=CC=CC=1.CC#N>[F:1][C:2]([C:5]1[N:10]=[CH:9][CH:8]=[CH:7][N:6]=1)([F:11])[CH2:3][I:36]
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참가 물질

7

반응물 4

HCID 795ImidazoleHCID 807IodineHCID 11776TriphenylphosphineHCID 589729572-Pyrimidineethanol, beta,beta-difluoro-

생성물 1

HCID 58973005Pyrimidine, 2-(1,1-difluoro-2-iodoethyl)-수율 73%

시약·촉매·용매 2

HCID 1140Toluene용매
HCID 6342
Acetonitrile
용매

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온도
0 °C

실험 절차

A homogeneous solution of 2,2-difluoro-2-pyrimidin-2-yl-ethanol (689 mg, 4.31 mmol), as prepared in the previous step, PPh3 (1.69 g, 6.44 mmol), and imidazole (590 mg, 8.67 mmol) in toluene (5.8 mL) and CH3CN (2.9 mL) was stirred at 0° C. for 5 min, and was then treated with I2 (1.61 g, 6.34 mmol) in two portions and stirred at 0° C. for another 5 min. The resulting brown opaque slurry was then heated at 90° C. for 19 h, and then allowed to cool to rt. The mixture was filtered, the beige filter cake was washed with toluene (3×10 mL), and the combined brown filtrates were concentrated. Silica flash chromatography of the residue (2:1 hex/EtOAc eluent) afforded the title compound as a pale yellow oil (849 mg, 73%).

후처리

  1. stirringstirred at 0° C. for another 5 min
  2. temperatureThe resulting brown opaque slurry was then heated at 90° C. for 19 h
  3. temperatureto cool to rt
  4. filtrationThe mixture was filtered
  5. washthe beige filter cake was washed with toluene (3×10 mL)
  6. concentrationthe combined brown filtrates were concentrated

출처 및 근거

ORD 기록
ord-2a5d9b66031e426f860c36afcf83578d
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07829584B2

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