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Sodium Carbonate → 4-Fluoro-3-(5-formylpyridin-2-yl)benzamide

HRID 561353
Notes
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Reaction equation

HRID 561353 reaction equation
Br[C:2]1[N:7]=[CH:6][C:5]([CH:8]=[O:9])=[CH:4][CH:3]=1.[C:10]([C:13]1[CH:14]=[CH:15][C:16]([F:22])=[C:17](B(O)O)[CH:18]=1)(=[O:12])[NH2:11].C([O-])([O-])=O.[Na+].[Na+]>COCCOC.CCO>[F:22][C:16]1[CH:17]=[CH:18][C:13]([C:10]([NH2:11])=[O:12])=[CH:14][C:15]=1[C:2]1[CH:3]=[CH:4][C:5]([CH:8]=[O:9])=[CH:6][N:7]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 10340Sodium CarbonateHCID 117692346-Bromo-3-pyridinecarboxaldehydeHCID 447174785-Carbamoyl-2-fluorobenzeneboronic acid

Product 1

HCID 595448574-Fluoro-3-(5-formylpyridin-2-yl)benzamide

Reagents, catalysts & solvents 2

HCID 702EthanolSolvent
HCID 8071
1,2-Dimethoxyethane
Solvent

Conditions

Temperature
80 °C

Procedure

To a solution of 6-bromo-3-pyridinecarboxaldehyde (336 mg, 1.80 mmol) in DME (8 mL) and EtOH (4 mL) under argon, was added (5-carbamoyl-2-fluorophenyl)boronic acid (300 mg, 1.64 mmol) followed by palladium tetrakistriphenylphosphine (190 mg, 0.16 mmol) and 2M Na2CO3 (4 mL). The mixture was heated to 80° C. for 16 h and then allowed to cool to rt. The mixture was partitioned between EtOAc (50 mL), THF (50 mL) and Na2CO3 (20 mL). The aqueous was extracted with EtOAc (50 mL) and the combined organics washed with brine (30 mL) and dried (MgSO4). The solvent was removed in vacuo and the residue purified by column chromatography (0.4% NH3: 4% MeOH: DCM) to give the title compound: RT=2.50 min; m/z (ES+)=245.0 [M+H]+.

Workup

  1. temperatureto cool to rt
  2. customThe mixture was partitioned between EtOAc (50 mL), THF (50 mL) and Na2CO3 (20 mL)
  3. extractionThe aqueous was extracted with EtOAc (50 mL)
  4. washthe combined organics washed with brine (30 mL)
  5. dry with materialdried (MgSO4)
  6. customThe solvent was removed in vacuo
  7. customthe residue purified by column chromatography (0.4% NH3: 4% MeOH: DCM)

Sources & evidence

ORD record
ord-d5279430e619446fa15f96da43a65166
Source dataset
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08063247B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes