Potassium Carbonate → 5-ethyl-2-(2'-fluoro-4'-methyl-3'-trifluoromethylanilino)phenylacetic acid N,N-dimethyl amide

HRID 1811539Notes

Reaction equation

HRID 1811539 reaction equation
[CH3:1][N:2]([CH3:15])[C:3](=[O:14])[CH2:4][C:5]1[CH:10]=[C:9]([CH2:11][CH3:12])[CH:8]=[CH:7][C:6]=1I.[F:16][C:17]1[C:24]([C:25]([F:28])([F:27])[F:26])=[CH:23][CH:22]=[CH:21][C:18]=1[NH:19]C.[C:29]([O-])([O-])=O.[K+].[K+]>CCOC(C)=O.[Cu]>[CH3:1][N:2]([CH3:15])[C:3](=[O:14])[CH2:4][C:5]1[CH:10]=[C:9]([CH2:11][CH3:12])[CH:8]=[CH:7][C:6]=1[NH:19][C:18]1[CH:21]=[CH:22][C:23]([CH3:29])=[C:24]([C:25]([F:28])([F:27])[F:26])[C:17]=1[F:16]

Participants

6

Reactant 3

HCID 11430Potassium CarbonateHCID 21938643N,N-dimethyl-5-ethyl-2-iodophenylacetamideHCID 688217352-fluoro-N-methyl-3-(trifluoromethyl)aniline

Product 1

HCID 689983795-ethyl-2-(2'-fluoro-4'-methyl-3'-trifluoromethylanilino)phenylacetic acid N,N-dimethyl amide

Reagents, catalysts & solvents 2

HCID 23978CopperCatalystHCID 8857Ethyl AcetateSolvent

Procedure

A mixture of N,N-dimethyl-5-ethyl-2-iodophenylacetamide (2.0 g, 6.3 mmol), 2-fluoro-methyl-3-trifluoromethylaniline (2.4 g, 12.6 mmol), copper (0.2 g, 3.2 mmol), cuprous iodide (0.6 g, 3.2 mmol), and K2CO3 (0.9 g, 6.3 mmol) in xylenes (6.0 mL) are heated at reflux for 24 h. After cooling, the crude reaction mixture is diluted with EtOAc and filtered through Celite®. The filtrate is concentrated under reduced pressure. The residue is purified by flash chromatography, eluting with hexanes, then up to 25% EtOAc/hexane mixtures to give the target compound 5-ethyl-2-(2′-fluoro-4′-methyl-3′-trifluoromethylanilino)phenylacetic acid N,N-dimethyl amide.

Workup

  1. temperatureare heated
  2. temperatureat reflux for 24 h
  3. temperatureAfter cooling
  4. customthe crude reaction mixture
  5. filtrationfiltered through Celite®
  6. concentrationThe filtrate is concentrated under reduced pressure
  7. customThe residue is purified by flash chromatography
  8. washeluting with hexanes

Sources & evidence

ORD record
ord-c0e30b4f5a8c4417bc84e788391df1c8
Source dataset
uspto-grants-2013_01
Patent number
US08362294B2

Reaction notes

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