Ammonia → HCID 11482748, compound

HRID 917748Notes

Reaction equation

HRID 917748 reaction equation
[NH3:1].[F:2][C:3]1[CH:31]=[C:30]([CH3:32])[CH:29]=[CH:28][C:4]=1[NH:5][C:6]1[C:7]([C:14](OC2C(F)=C(F)C(F)=C(F)C=2F)=[O:15])=[CH:8][N:9]([CH3:13])[C:10](=[O:12])[CH:11]=1>C1COCC1>[F:2][C:3]1[CH:31]=[C:30]([CH3:32])[CH:29]=[CH:28][C:4]=1[NH:5][C:6]1[C:7]([C:14]([NH2:1])=[O:15])=[CH:8][N:9]([CH3:13])[C:10](=[O:12])[CH:11]=1

Participants

4

Reactant 2

HCID 222AmmoniaHCID 58962850HCID 58962850, compound

Product 1

HCID 11482748HCID 11482748, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

Conc. NH3 solution (0.5 ml) was added to 2,3,4,5,6-pentafluorophenyl 4-(2-fluoro-4-methylanilino)-1-methyl-6-oxo-1,6-dihydro-3-pyridinecarboxylate (0.33 g, 0.6 mmol) in THF (10 ml) and the solution stirred at RT for 2 h. The solvent was removed under reduced pressure and the residue dissolved in 5% EtOAc/MeOH. The organic phase was washed with water, brine, dried (Na2SO4) and concentrated to give crude 4-(2-fluoro-4-methylanilino)-1-methyl-6-oxo-1,6-dihydro-3-pyridinearboxamide which was then recrystallised (EtOAc/Hexane) (0.11 g, 84%); m.p. (EtOAc/Hexane) 285-288° C. 1H NMR [400 MHz, (CD3)2SO] δ 10.14 (s, 1H), 8.32 (s, 1H), 7.86 (br s, 1H), 7.43 (br s, 1H), 7.31 (t, J=8.4 Hz), 1H), 7.16 (dd, J=11.8, 1.1 Hz, 1H), 7.05 (d, J=8.2 Hz, 1H), 5.38 (d, J=1.1 Hz, 1H), 3.34 (s, 3H), 2.32 (s, 3H). LCMS (ACPI−) 274 (100%). Anal. Calcd for C14H14FN3O2: C, 61.1; H, 5.1; N, 15.3. Found C, 61.0; H, 5.2; N, 15.4.

Workup

  1. customThe solvent was removed under reduced pressure
  2. dissolutionthe residue dissolved in 5% EtOAc/MeOH
  3. washThe organic phase was washed with water, brine
  4. dry with materialdried (Na2SO4)
  5. concentrationconcentrated
  6. customto give crude 4-(2-fluoro-4-methylanilino)-1-methyl-6-oxo-1,6-dihydro-3-pyridinearboxamide which
  7. customwas then recrystallised (EtOAc/Hexane) (0.11 g, 84%)
  8. customm.p. (EtOAc/Hexane) 285-288° C

Sources & evidence

ORD record
ord-7f64bcb2868d4377b1be1a9ba02a7981
Source dataset
uspto-grants-2007_09
Patent number
US07273877B2

Reaction notes

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