반응 #314409

ord-036db8a18ee341ed87f1a28b6714d5e1

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGstirred at 20° C. for 1 hour
  2. 2
    workup.STIRRINGstirred at 20° C. for 1 hour
  3. 3
    workup.STIRRINGthen stirred for 5 hours
  4. 4
    건조the organic phase dried (magnesium sulfate)
  5. 5
    기타evaporated
  6. 6
    기타the residue purified by silica gel column chromatography
  7. 7
    세척eluting with n-hexane/ethyl acetate (3:1)

실험 절차

Sodium hydride (0.09 g, 60% dispersion in mineral oil) was added portionwise to a solution of 4-trifluoromethyl-3-pyridinecarboxamide (0.40 g) in N,N-dimethylformamide at 20° C., and stirred for 1 hour. Benzyl isothiocyanate (0.31 ml) was added and stirred at 20° C. for 1 hour, then 1,2-dibromoethane (0.30 ml) added and stirred at 20° C. for 1 hour. Sodium hydride (0.09 g, 60% dispersion in mineral oil) was added in portions to the solution then stirred for 5 hours. Ethyl acetate and water were added, the organic phase dried (magnesium sulfate), evaporated and the residue purified by silica gel column chromatography eluting with n-hexane/ethyl acetate (3:1) to give 3-benzyl-2-(4-trifluoromethyl-3-pyridylcarbonyl)iminothiazolidine (0.50 g, Compound D-40).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07560456B2uspto-grants-2009_07