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Methanol → HCID 67304384, compound

HRID 860143
Notes
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Reaction equation

HRID 860143 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH:12]=[C:11]([C:13](O)=[O:14])[N:10]=[CH:9]2)=[CH:4][CH:3]=1.O1CCCC1.B.CO>C1COCC1>[F:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[CH:12]=[C:11]([CH2:13][OH:14])[N:10]=[CH:9]2)=[CH:6][CH:7]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 887MethanolHCID 2723981Borane;tetrahydrofuranHCID 173900481-(4-Fluorophenyl)-1H-imidazole-4-carboxylic acid

Product 1

HCID 67304384HCID 67304384, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

1-(4-Fluoro-phenyl)-1H-imidazole-4-carboxylic acid (18 g, 87 mmol) was dissolved in 90 mL dry THF. Borane tetrahydrofuran complex (174 mL, 1M in THF, 174 mmol) was added dropwise. The reaction was refluxed for 2 h and stirred at RT overnight. The reaction mixture was cooled to 0° C. and 100 mL methanol were added dropwise. The solvents were evaporated. The residue was taken up in 100 mL 2N HCl and refluxed for 2 h. The reaction mixture was then cooled to 0° C. and 120 mL 2N sodium hydroxide solution were added dropwise. The solid material was filtered off and dried at 50° C. and 15 mbar. The desired compound was obtained as a white solid (13 g, 78%), MS: m/e=193.2 (M+H)+.

Workup

  1. temperatureThe reaction was refluxed for 2 h
  2. temperatureThe reaction mixture was cooled to 0° C.
  3. customThe solvents were evaporated
  4. temperaturerefluxed for 2 h
  5. temperatureThe reaction mixture was then cooled to 0° C.
  6. addition120 mL 2N sodium hydroxide solution were added dropwise
  7. filtrationThe solid material was filtered off
  8. customdried at 50° C.

Sources & evidence

ORD record
ord-bc99bd583ccf4b9cb4846441b1fa6eed
Source dataset
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07153874B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes