Réaction #44153

ord-31b68b25b74944dfa858c3c525522868

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrepartitioned between saturated aqueous sodium hydrogencarbonate solution and DCM
  2. 2
    LavageThe organic layer was washed with water
  3. 3
    Autredried
  4. 4
    Concentrationconcentrated in vacuo
  5. 5
    AutreThe residue was purified by column chromatography [SiO2; DCM-MeOH, (20:0)→(20:1)]

Mode opératoire

To a stirred solution of 3-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]ethyl}aniline (370 mg) and triethylamine (178 μL) in DCM (3 mL) was added methanesulfonyl chloride (33 L). The mixture was stirred for 18 h, then partitioned between saturated aqueous sodium hydrogencarbonate solution and DCM. The organic layer was washed with water, dried and concentrated in vacuo. The residue was purified by column chromatography [SiO2; DCM-MeOH, (20:0)→(20:1)] to give the title compound (342 mg).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07732600B2uspto-grants-2010_06