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

HRID 1474048
Notes
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Reaction equation

HRID 1474048 reaction equation
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]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

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

Product 1

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

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-5974b022c14944089161837bbf37db24
Source dataset
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09018217B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes