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Potassium Carbonate → Ethyl 5-(2,2-difluoroethoxy)-3-fluoro-pyridine-2-carboxylate

HRID 571748
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HRID 571748 반응식
[F:1][C:2]1[C:3]([C:9]([O:11][CH2:12][CH3:13])=[O:10])=[N:4][CH:5]=[C:6](F)[CH:7]=1.[F:14][C:15]([F:18])(O)[CH3:16].C(=O)([O-])[O-:20].[K+].[K+]>C(#N)C>[F:14][CH:15]([F:18])[CH2:16][O:20][C:6]1[CH:7]=[C:2]([F:1])[C:3]([C:9]([O:11][CH2:12][CH3:13])=[O:10])=[N:4][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 20243757DifluoroethanolHCID 46311358Ethyl 3,5-difluoropyridine-2-carboxylate

생성물 1

HCID 117738010Ethyl 5-(2,2-difluoroethoxy)-3-fluoro-pyridine-2-carboxylate수율 18.5%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

Ethyl 3,5-difluoropyridine-2-carboxylate (0.98 g, 5.24 mmol) is dissolved in acetonitrile (20 mL). Difluoroethanol (430 μL, 6.81 mmol) is added followed by potassium carbonate (1.83 g, 13.09 mmol). The solution is stirred at room temperature for 2 days then filtered and the filtrate is concentrated. The crude material is purified via silica gel chromatography eluting with a 0-25-50% ethyl acetate/hexanes gradient to give the title compound (242 mg, 18%). ES/MS (m/e): 250.0 (M+1).

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후처리

  1. filtrationthen filtered
  2. concentrationthe filtrate is concentrated
  3. customThe crude material is purified via silica gel chromatography
  4. washeluting with a 0-25-50% ethyl acetate/hexanes gradient

출처 및 근거

ORD 기록
ord-048dc71082c740338c79e73032d81353
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09029367B2

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