Реакция #417984

ord-72af8d8b58344a33b57e2ec1935b028b

Уравнение реакции

CC(C)(C)OC(=O)N1CCC(COc2cnc(-c3cccc(Cn4c(=O)sc5ccc(C(F)(F)F)cc54)c3)nc2)CC1
3-{3-[5-(1-tert-butoxycarbonylpiperidin-4-yl-methoxy)pyrimidin-2-yl]benzyl}-5-trifluoromethyl-3H-benzothiazol-2-one
Cl
HCl
O=c1sc2ccc(C(F)(F)F)cc2n1Cc1cccc(-c2ncc(OCC3CCNCC3)cn2)c1
3-{3-[5-(piperidin-4-ylmethoxy)pyrimidin-2-yl]benzyl}-5-trifluoromethyl-3H-benzothiazol-2-one

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияA viscous precipitate forms in the process, which is filtered off with suction
  2. 2
    workup.STIRRINGstirred with isopropanol

Методика

424 mg (0.64 mmol) of 3-{3-[5-(1-tert-butoxycarbonylpiperidin-4-yl-methoxy)pyrimidin-2-yl]benzyl}-5-trifluoromethyl-3H-benzothiazol-2-one is dissolved in 20 ml of dioxane, and 6 ml of 4N HCl in dioxane are added. The mixture is stirred at room temperature for 24 h. A viscous precipitate forms in the process, which is filtered off with suction and stirred with isopropanol.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08877751B2uspto-grants-2014_11