반응 #59797

ord-c028a1774c4c45dd938a698fb5c8d8e4

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도cooled in an ice bath
  2. 2
    기타The solvent was evaporated
  3. 3
    기타The mixture was sonicated
  4. 4
    workup.WAITto stand at ambient temperature overnight
  5. 5
    세척washed with water
  6. 6
    기타The organic portion was separated
  7. 7
    기타evaporated
  8. 8
    기타to give the crude urea
  9. 9
    기타Purification of the crude urea by flash chromatography (silica gel)

실험 절차

[4,5-Bis-(4-chloro-phenyl)-2-(2-ethoxy-4-trifluoromethyl-phenyl)-4,5-dihydro-imidazol-1-yl]-piperazin-1-yl-methanone (50 mg, 0.085 mmol, example 8A) was dissolved in methylene chloride (1 mL) and cooled in an ice bath. Phosgene (250 uL, 20% solution in toluene)) was added, and the mixture was stirred for 30 min. The solvent was evaporated and the residue was taken in methylene chloride. One third of this solution (0.028 mmol) was treated with 2-piperazinone (8.5 mg) and diisopropylethylamine (15 ul). The mixture was sonicated to aid in dissolving the amine and allowed to stand at ambient temperature overnight. It was diluted with methylene chloride and washed with water. The organic portion was separated and evaporated to give the crude urea. Purification of the crude urea by flash chromatography (silica gel) using ethyl acetate and hexanes gave 4-{4-[4,5-bis-(4-chloro-phenyl)-2-(2-ethoxy-4-trifluoromethyl-phenyl)-4,5-dihydro-imidazole-1-carbonyl]-piperazine-1-carbonyl}-piperazin-2-one (9.0 mg). LR-MS: 718.4 [(M+H)+].

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07425638B2uspto-grants-2008_09