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1-Propanol → Pyrazolo[1,5-a]pyridin-2-ylmethanol

HRID 1474048
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HRID 1474048 반응식
N=[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]1[NH:8]C(N1C=CN=C1)=S.ClCC1N(C)C=C(C2C=CC=CC=2)N=1.[CH2:30]([OH:33])[CH2:31][CH3:32]>>[N:8]1[N:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]2=[CH:32][C:31]=1[CH2:30][OH:33]
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참가 물질

4

반응물 3

HCID 10311-PropanolHCID 15334493Imidazole-1-carbothioic acid (2-imino-2H-pyridin-1-yl)-amideHCID 591512282-Chloromethyl-1-methyl-4-phenyl-1H-imidazole

생성물 1

HCID 12669575Pyrazolo[1,5-a]pyridin-2-ylmethanol수율 62%

실험 절차

An adaptation of the method described in WO 96/01826 was used. Imidazole-1-carbothioic acid (2-imino-2H-pyridin-1-yl)-amide (200 mg, 1.37 mmol) and 2-chloromethyl-1-methyl-4-phenyl-1H-imidazole 6 (300 mg, 1.46 mmol) were dissolved in 1-propanol (25 mL) and the mixture was heated to reflux for 2 hours. The solvent was removed under reduced pressure and the residue dissolved in dichloromethane. The solution was washed with water and the organic layer was dried over Na2SO4 and concentrated. The residue was purified by chromatography on silica gel to afford the title compound (273 mg, 62%) as a yellow solid. LC-MS: m/z=322.1 (MH+), tR=2.29 min, method B.

후처리

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 2 hours
  3. customThe solvent was removed under reduced pressure
  4. dissolutionthe residue dissolved in dichloromethane
  5. washThe solution was washed with water
  6. dry with materialthe organic layer was dried over Na2SO4
  7. concentrationconcentrated
  8. customThe residue was purified by chromatography on silica gel

출처 및 근거

ORD 기록
ord-5974b022c14944089161837bbf37db24
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09018217B2

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