Реакция #2320075

ord-436286d3dc684c20b402a4250ffaf3cf

Уравнение реакции

FC(F)(F)c1cc(Br)ccc1Cl
5-bromo-2-chlorobenzotrifluoride
CCCN1CCNCC1
n-propyl piperazine
CC(C)(C)[O-].[Na+]
sodium tert-butoxide
CCCN1CCN(c2ccc(Cl)c(C(F)(F)F)c2)CC1
1-(4-Chloro-3-trifluoromethyl-phenyl)-4-propyl-piperazine

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Промывкаwashed with brine (15-20 ml)
  2. 2
    СушкаThe organic fraction was dried (MgSO4)
  3. 3
    Фильтрацияfiltered
  4. 4
    Другоеevaporated to dryness
  5. 5
    ДругоеThe crude material was purified by flash chromatography on silica gel
  6. 6
    Другоеrecrystallized from ethanol/diethylether

Методика

A mixture of 5-bromo-2-chlorobenzotrifluoride (0.2 g, 0.85 mmol), n-propyl piperazine (0.15 g, 1.17 mmol), sodium tert-butoxide (0.134 g) dppf (14 mg) and [Pd2(dba)3 (10 mg) in dioxane (5 ml) was heated under argon at 100° C. for 24 h. After cooling to room temperature, the reaction mixture was taken up in Et2O (40-50 ml) and washed with brine (15-20 ml). The organic fraction was dried (MgSO4), filtered and evaporated to dryness. The crude material was purified by flash chromatography on silica gel using CH2Cl2:MeOH (9:1 (v/v)). The amine was converted into the HCl-salt and recrystallized from ethanol/diethylether; m.p. 268° C. (HCl); MS m/z (rel. intensity, 70 eV)) 307 (M+, 6), 279 (33), 277 (98), 70 (bp), 56 (40). Rf=0.35 (EtOAc)

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE041315E1uspto-grants-2010_05