Reaction #436674

ord-e69efc08d36c4b00a54b442bca9c5101

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherat room temperature
  2. 2
    Temperaturerefluxed for 5 min
  3. 3
    Extractionextracted with ethyl acetate
  4. 4
    Concentrationthe extract was concentrated under a reduced pressure
  5. 5
    OtherThe resulting residue was purified by silica gel column chromatography

Procedure

3-[(2-chloro-4-fluoro-benzimidoyl)-amino]-4-methoxy-benzoic acid methyl ester (10 g, 29.76 mmol) obtained in step 1 was dissolved in 50% methanol and 5% NaOCl (53 ml, 35.71 mmol) was added dropwise thereto at room temperature. After 5 min, Na2CO3 (6.31 g, 59.52 mmol) was added dropwise thereto and refluxed for 5 min. The resulting solution was cooled to room temperature, extracted with ethyl acetate, the extract was concentrated under a reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound (5.17 g, 15.48 mmol) in a yield of 52%.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07179832B2uspto-grants-2007_02