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Water → (2-Ethyl-pyrazolo[1,5-a]pyridin-3-yl)methanol

HRID 1802747
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반응식

HRID 1802747 반응식
C([O:3][C:4]([C:6]1[C:7]([CH2:15][CH3:16])=[N:8][N:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=12)=O)C.[H-].[Al+3].[Li+].[H-].[H-].[H-].O>O1CCCC1>[CH2:15]([C:7]1[C:6]([CH2:4][OH:3])=[C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][N:9]2[N:8]=1)[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 137381512-Ethyl-pyrazolo[1,5-a]pyridine-3-carboxylic acid ethyl esterHCID 21226445Aluminium lithium hydride

생성물 1

HCID 57899265(2-Ethyl-pyrazolo[1,5-a]pyridin-3-yl)methanol수율 80%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 2-ethyl-pyrazolo[1,5-a]pyridine-3-carboxylic acid ethyl ester (15 g, 68.7 mmol) in tetrahydrofuran (300 mL) was cooled in an ice bath and lithium aluminum hydride (2.6 g, 68.7 mmol) was added. The reaction mixture was stirred at room temperature for 16 h. Water was added until bubbling stopped. Silica gel was added and the solvent was evaporated in vacuo. The resulting residue was purified via silica chromatography (20-100% ethyl acetate/heptane) to yield the title compound as a yellow/brown oil (9.67 g, 80% yield).

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후처리

  1. customuntil bubbling
  2. additionSilica gel was added
  3. customthe solvent was evaporated in vacuo
  4. customThe resulting residue was purified via silica chromatography (20-100% ethyl acetate/heptane)

출처 및 근거

ORD 기록
ord-3c5cefecdcfe465da5b1fdfa1119cba0
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08349883B2

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