Реакция #340950

ord-eb6fc9d005a04ae4824652d9de50fb78

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONwas added
  2. 2
    СушкаThe organic phase was dried (MgSO4)
  3. 3
    Другоеthe solvent was removed in vacuo
  4. 4
    workup.ADDITIONMeCN (1 mL) was added whereupon the product
  5. 5
    Другоеprecipitated
  6. 6
    ФильтрацияThe product was filtered off
  7. 7
    Другоеdried

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07872139B2uspto-grants-2011_01