Ethanol → HCID 21875914, compound

HRID 724146Notes

Reaction equation

HRID 724146 reaction equation
[NH2:1][C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[C:5]([Cl:12])=[CH:4][C:3]=1[NH:13][C:14]1[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][OH:22])=[CH:16][CH:15]=1.[N:23]1[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=1[CH:29]=O.CCO>CCOC(C)=O>[Cl:12][C:5]1[C:6]([C:8]([F:10])([F:11])[F:9])=[CH:7][C:2]2[N:1]=[C:29]([C:24]3[CH:25]=[CH:26][CH:27]=[CH:28][N:23]=3)[N:13]([C:14]3[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][OH:22])=[CH:16][CH:15]=3)[C:3]=2[CH:4]=1

Participants

5

Procedure

A mixture of 2-(4-{[2-amino-5-chloro-4-(trifluoromethyl)phenyl]amino}phenyl)ethanol (1.83 g, 5.54 mmol), 2-pyridinecarboxaldehyde (0.53 ml, 5.54 mmol), and EtOH (40 ml) was refluxed for 1 hour. After cooling to room temperature, the solvent was removed. The residue was dissolved with benzene (50 ml) and treated with Pb(OAc)4 (3.38 g, 6.10 mmol) at room temperature for 1 hour. The mixture was diluted with EtOAc and the solution was washed with sat. NaHCO3 aq. and brine. The organic fraction was dried over MgSO4, then filtered. After evaporation in vacuo, the residue was purified by silica-gel column chromatography eluting with hexane/EtOAc=5/2 to afford 1.20 g (52%) of the title compound.

Workup

  1. temperaturewas refluxed for 1 hour
  2. customthe solvent was removed
  3. dissolutionThe residue was dissolved with benzene (50 ml)
  4. washthe solution was washed with sat. NaHCO3 aq. and brine
  5. dry with materialThe organic fraction was dried over MgSO4
  6. filtrationfiltered
  7. customAfter evaporation in vacuo
  8. customthe residue was purified by silica-gel column chromatography
  9. washeluting with hexane/EtOAc=5/2

Sources & evidence

ORD record
ord-ca2ce3e5249a4c268eae766ebac1040d
Source dataset
uspto-grants-2006_11
Patent number
US07141580B2

Reaction notes

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