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Sodium Bicarbonate → 3-(5-Fluoro-pyridin-2-yl)-5-methyl-isoxazole-4-carbaldehyde

HRID 1923571
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HRID 1923571 반응식
[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[C:12]([CH2:13][OH:14])=[C:11]([CH3:15])[O:10][N:9]=2)=[N:6][CH:7]=1.C(=O)([O-])O.[Na+]>C(Cl)Cl>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[C:12]([CH:13]=[O:14])=[C:11]([CH3:15])[O:10][N:9]=2)=[N:6][CH:7]=1
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참가 물질

4

반응물 2

HCID 516892Sodium BicarbonateHCID 66599256[3-(5-Fluoro-pyridin-2-yl)-5-methyl-isoxazol-4-yl]-methanol

생성물 1

HCID 866472723-(5-Fluoro-pyridin-2-yl)-5-methyl-isoxazole-4-carbaldehyde수율 90.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

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온도
0 °C

실험 절차

To a solution of [3-(5-fluoro-pyridin-2-yl)-5-methyl-isoxazol-4-yl]-methanol (1.9 g, 9.13 mmol) in DCM (38 mL) was added a suspension of DMP (4.65 g, 10.96 mmol) in DCM (30 mL) portionwise and under argon at room temperature and then the mixture was cooled to 0° C. and the resulting mixture warmed up to room temperature overnight. The mixture was then poured carefully into stirred saturated sodium hydrogen carbonate solution and the aqueous layer extracted with DCM. The combined organic layers were then washed with brine, dried over sodium sulfate and evaporated. Purification by chromatography (silica, 0 to 50% ethyl acetate in heptane) gave the title compound (1.7 g, 90%) as a white solid. MS: m/e=207.0 [M+H]+. Alternatively

후처리

  1. temperaturethe resulting mixture warmed up to room temperature overnight
  2. additionThe mixture was then poured carefully
  3. extractionthe aqueous layer extracted with DCM
  4. washThe combined organic layers were then washed with brine
  5. dry with materialdried over sodium sulfate
  6. customevaporated
  7. customPurification by chromatography (silica, 0 to 50% ethyl acetate in heptane)

출처 및 근거

ORD 기록
ord-6dc6a7208984451d897bda32eba4f9f3
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08178522B2

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