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3,5-Difluoropyridine-2-carboxylic acid → 3,5-difluoro-N-methylpyridine-2-carboxamide

HRID 389098
Notes
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Reaction equation

HRID 389098 reaction equation
[F:1][C:2]1[C:3]([C:9]([OH:11])=O)=[N:4][CH:5]=[C:6]([F:8])[CH:7]=1.[CH3:12][NH2:13].CO>C1COCC1>[F:1][C:2]1[C:3]([C:9]([NH:13][CH3:12])=[O:11])=[N:4][CH:5]=[C:6]([F:8])[CH:7]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 27832623,5-Difluoropyridine-2-carboxylic acidHCID 57454252Monomethylamine methanol

Product 1

HCID 582437773,5-difluoro-N-methylpyridine-2-carboxamide

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
50 °C

Procedure

N,N′-carbonyldiimidazole (600 mg) was added to a solution of 3,5-difluoropyridine-2-carboxylic acid (500 mg) in THF (10 ml), followed by stirring at 50° C. for one hour. The reaction solution was returned to room temperature, a 40% methylamine/methanol solution (1 ml) was added thereto, followed by stirring at room temperature for one hour. The reaction solution was concentrated and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=100:0 to 0:100 linear gradient) to obtain 3,5-difluoro-N-methylpyridine-2-carboxamide (293 mg) as a colorless solid.

Workup

  1. customwas returned to room temperature
  2. stirringby stirring at room temperature for one hour
  3. concentrationThe reaction solution was concentrated
  4. customthe residue was purified by silica gel column chromatography (hexane:ethyl acetate=100:0 to 0:100 linear gradient)

Sources & evidence

ORD record
ord-542ff3a5fff6400e99c84b91f9847ebe
Source dataset
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08377923B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes