Réaction #340950

ord-eb6fc9d005a04ae4824652d9de50fb78

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONwas added
  2. 2
    SéchageThe organic phase was dried (MgSO4)
  3. 3
    Autrethe solvent was removed in vacuo
  4. 4
    workup.ADDITIONMeCN (1 mL) was added whereupon the product
  5. 5
    Autreprecipitated
  6. 6
    FiltrationThe product was filtered off
  7. 7
    Autredried

Mode opératoire

1-Cyclohexyl-1-piperidin-1-yl-3-thiazol-2-yl-urea (50 mg, 0.16 mmol), prepared in an identical manner to Example 94 was dissolved in DCM (1 mL) and NCS (26 mg, 0.19 mmol)) was added. The reaction mixture was stirred for 3 days before DCM (20 mL) and water (20 mL) was added. The organic phase was dried (MgSO4) and the solvent was removed in vacuo. MeCN (1 mL) was added whereupon the product precipitated. The product was filtered off and dried. Yield: 20 mg.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07872139B2uspto-grants-2011_01