반응 #535755

ord-eff6a95bd1824e58b8cf1ce49b43bbe9

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타the solvent was removed
  2. 2
    온도40 mL of toluene and cooled to 0° C
  3. 3
    workup.ADDITIONIsopropyl chloroformate (60 mL of a 1 M solution in toluene, 1.2 eq) and diisopropylethylamine (24 mL) were added
  4. 4
    workup.STIRRINGThe mixture was stirred for 36 h
  5. 5
    세척washed with 1 M HCl (3×100 mL), 100 mL of water and 100 mL of brine
  6. 6
    기타The solvent was evaporated
  7. 7
    온도cooled at 0° C.
  8. 8
    workup.STIRRINGstirred for 2 h
  9. 9
    기타to give a precipitate which
  10. 10
    여과was filtered
  11. 11
    세척washed with hexane

실험 절차

9a was dissolved in a 4 M solution of HCl in dioxane (60 mL). The solution was stirred at room temperature for 3 h and the solvent was removed. The residue was taken up in 200 mL of DCM and 40 mL of toluene and cooled to 0° C. Isopropyl chloroformate (60 mL of a 1 M solution in toluene, 1.2 eq) and diisopropylethylamine (24 mL) were added. The mixture was stirred for 36 h, washed with 1 M HCl (3×100 mL), 100 mL of water and 100 mL of brine. The solvent was evaporated and the residue taken up in 50 mL of hexane, cooled at 0° C. and stirred for 2 h to give a precipitate which was filtered and washed with hexane. 2.89 g of 9b were obtained. The filtrate was concentrated and recrystallized with IPA. Some light yellow crystals were obtained, filtered and washed with IPA to give 3.38 g of 9b. The filtrate was concentrated and purified on silica gel (eluent: 20% ethyl acetate in hexane) to give 2.2 g of 9b. Total yield of 9b: 8.47 g (54%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08481731B2uspto-grants-2013_07