Sodium Carbonate → Methyl 2-(4-fluorophenyl)nicotinate

HRID 1242667Notes

Reaction equation

HRID 1242667 reaction equation
C(=O)([O-])[O-].[Na+].[Na+].[CH3:7][O:8][C:9](=[O:17])[C:10]1[CH:15]=[CH:14][CH:13]=[N:12][C:11]=1Cl.[F:18][C:19]1[CH:24]=[CH:23][C:22](B(O)O)=[CH:21][CH:20]=1>CCO>[CH3:7][O:8][C:9](=[O:17])[C:10]1[CH:15]=[CH:14][CH:13]=[N:12][C:11]=1[C:22]1[CH:23]=[CH:24][C:19]([F:18])=[CH:20][CH:21]=1

Participants

5

Reactant 3

HCID 10340Sodium CarbonateHCID 2856454-Fluorophenylboronic acidHCID 819931Methyl 2-chloronicotinate

Product 1

HCID 15318001Methyl 2-(4-fluorophenyl)nicotinate

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Conditions

Temperature
78 °C

Procedure

To a nitrogen purged flask was charged Pd(Ph3)4 (1.84 g, 1.6 mmoles, 0.005 eq), sodium carbonate (42.8 g, 404 mmoles, 1.3 eq), 52 (55.5 g, 320.6 mmoles, 1.0 eq), p-fluorophenylboronic acid (53.8 g, 384.7 mmoles, 1.2 eq), followed by 1.3 L denatured EtOH. The reaction was heated to 78° C. with vigorous stirring under N2 overnight. HPLC analysis [Tret 52=10 min, Tret 54=12 min] of the reaction mixture showed that the starting material was completely consumed and a later-eluting peak produced. The reaction was cooled to room temperature and the solvents removed under vacuum. The residue was dissolved in EtOAc, washed, dried (MgSO4), filtered through celite, and concentrated to afford a pale yellow solid 54.

Workup

  1. customHPLC analysis [Tret 52=10 min, Tret 54=12 min] of the reaction mixture
  2. customwas completely consumed
  3. customa later-eluting peak produced
  4. temperatureThe reaction was cooled to room temperature
  5. customthe solvents removed under vacuum
  6. dissolutionThe residue was dissolved in EtOAc
  7. washwashed
  8. dry with materialdried (MgSO4)
  9. filtrationfiltered through celite
  10. concentrationconcentrated

Sources & evidence

ORD record
ord-e41745900f87450caba99a6c92282a23
Source dataset
uspto-grants-2006_10
Patent number
US07115746B2

Reaction notes

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