반응 #418310

ord-ff7aaf655f3d4a66a41eaa7ddc2c55ac

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척For the workup, the mixture was washed with saturated an aqueous solution of ammonium chloride
  2. 2
    기타The organic layer was dried
  3. 3
    기타evaporated at reduced pressure
  4. 4
    기타the residue was purified by chromatography on silica

실험 절차

To a solution of (R)-5-(5-bromo-2-fluorophenyl)-6,6-difluoro-5-methyl-2,5,6,7-tetrahydro-1,4-oxazepin-3-amine (intermediate A7.1) (9.0 mmol) in dichloromethane (150 ml) was subsequently added at 0° C. triethylamine (18.0 mmol) and 4,4′-dimethoxytriphenylmethyl chloride (9.9 mmol) and stirring was continued at 22° C. for 2 hours. For the workup, the mixture was washed with saturated an aqueous solution of ammonium chloride. The organic layer was dried, evaporated at reduced pressure, and the residue was purified by chromatography on silica using cyclohexane/ethyl acetate to give pure (R)—N-(bis(4-methoxyphenyl)(phenyl)methyl)-5-(5-bromo-2-fluorophenyl)-6,6-difluoro-5-methyl-2,5,6,7-tetrahydro-1,4-oxazepin-3-amine (A8.1) as a colorless foam. MS (ISP): m/z=639.3 [M+H]+ and 641.4 [M+2+H]+.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08877744B2uspto-grants-2014_11