반응 #69482

ord-190175ec38204e3e950aba4aa02ef4e8

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축After concentration, DCM (15 mL) and MeOH (15 mL)
  2. 2
    workup.ADDITIONwere added
  3. 3
    기타purified by flash chromatography on silica gel eluting with 0 to 10% methanol in DCM
  4. 4
    기타The solvent was evaporated to dryness
  5. 5
    기타to give a solid
  6. 6
    기타dried under vacuum

실험 절차

HCl 4M (9.74 mL, 39 mmol) was added to a stirred solution of tert-butyl 2-(6-(morpholine-4-carbonyl)-2-morpholino-4-oxo-4H-chromen-8-yl)pyrrolidine-1-carboxylate (2 g, 3.89 mmol) dissolved in DCM (15 mL) at r.t and stirred over the week-end. After concentration, DCM (15 mL) and MeOH (15 mL) were added, followed by a solution of 10% methanolic ammonia (7 N) in DCM (10 mL). The crude product was adsorbed on silica gel and purified by flash chromatography on silica gel eluting with 0 to 10% methanol in DCM. The solvent was evaporated to dryness to give a solid and dried under vacuum to give 6-(morpholine-4-carbonyl)-2-morpholino-8-(pyrrolidin-2-yl)-4H-chromen-4-one (1.0 g, 62%) as a beige solid. Mass Spectrum: m/z [M+H]+=414.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08530470B2uspto-grants-2013_09