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Tetrahydrofuran → 4-(Bromomethyl)-2-(1H-pyrazol-1-YL)pyridine

HRID 41587
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HRID 41587 반응식
[N:1]1([C:6]2[CH:11]=[C:10]([CH2:12]O)[CH:9]=[CH:8][N:7]=2)[CH:5]=[CH:4][CH:3]=[N:2]1.P(Br)(Br)[Br:15].C1COCC1.C([O-])(O)=O.[Na+]>C(OCC)C.C(OCC)(=O)C>[Br:15][CH2:12][C:10]1[CH:9]=[CH:8][N:7]=[C:6]([N:1]2[CH:5]=[CH:4][CH:3]=[N:2]2)[CH:11]=1
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참가 물질

7

반응물 4

HCID 8028TetrahydrofuranHCID 24614Phosphorus tribromideHCID 516892Sodium BicarbonateHCID 61256684(2-(1H-Pyrazol-1-YL)pyridin-4-YL)methanol

생성물 1

HCID 717423084-(Bromomethyl)-2-(1H-pyrazol-1-YL)pyridine수율 70%

시약·촉매·용매 2

HCID 3283Diethyl Ether
용매
HCID 8857Ethyl Acetate용매

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온도
65 °C

실험 절차

To a stirred solution of (2-(1H-pyrazol-1-yl)pyridin-4-yl)methanol (175 mg, 1.00 mmol) in diethyl ether (5 mL), PBr3 (0.11 mL, 1.00 mmol) was added dropwise at 0° C. Then THF (5 mL) was added to the resulting white precipitate and the mixture was heated at 65° C. for 1 h. The mixture was cooled to rt, diluted with ethyl acetate (5 mL) and poured into saturated aqueous NaHCO3 solution (5 mL). The layers were separated and the aqueous layer was extracted with ethyl acetate (2×5 mL). The combined organic layers were washed with brine and dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure to yield the title compound (165 mg, 70%). [LCMS RtE=1.33 min, [M+H]+=237.9/239.9].

후처리

  1. temperatureThe mixture was cooled to rt
  2. customThe layers were separated
  3. extractionthe aqueous layer was extracted with ethyl acetate (2×5 mL)
  4. washThe combined organic layers were washed with brine
  5. dry with materialdried over anhydrous Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-69bb823c750d4b289af34adcebfc2638
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08530648B2

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