Reaction #413998

ord-72a3ac04b851493ea94215da1553fec9

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Temperaturethe mixture was heated
  2. 2
    Temperatureunder reflux for 1 hour
  3. 3
    workup.DISTILLATIONThe solvent was distilled away under reduced pressure
  4. 4
    WashThe residue was washed with water
  5. 5
    Otherdried

Procedure

6 g of 1-(3-trifluoromethylbenzoyl)-1-methanesulfonyl-2-(N,N-dimethylamino)ethene and 4 g of 4-fluorobenzamidine hydrochloride were dissolved in 30 ml of methanol at room temperature. After adding 1.2 g of sodium methoxide thereto, the mixture was heated under reflux for 1 hour. The solvent was distilled away under reduced pressure. The residue was washed with water, and then dried to obtain 6 g of 2-(4-fluorophenyl)-4-(3-trifluoromethylphenyl)-5-methanesulfonylpyrimidine (Compound 112).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05270467uspto-grants-1993_12