반응 #326273

ord-e89087b9ecd44e4485861a175069ea7a

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas added
  2. 2
    여과The resulting slurry was filtered under suction
  3. 3
    세척washed with 2 mL of ethyl acetate
  4. 4
    기타dried under reduced pressure at room temperature
  5. 5
    workup.STIRRINGstirred at room temperature for 15.5 hrs
  6. 6
    여과The resulting slurry was filtered under suction
  7. 7
    세척washed with 2 mL of ethyl acetate
  8. 8
    기타dried under reduced pressure at room temperature

실험 절차

To ethyl acetate (5 mL) solution containing 251.0 mg of the mixture of (1R,2S,3R,5R,6R)-2-amino-2-cyano-3-[(3,4-dichloro benzyl)oxy]-6-fluoro bicyclo[3.1.0]hexane-6-carboxamide (6a) and (1R,2R,3R,5R,6R)-2-amino-2-cyano-3-[(3,4-dichloro benzyl)oxy]-6-fluoro bicyclo[3.1.0]hexane-6-carboxamide (8a) [containing (6a): 171.5 mg and (8a): 75.1 mg], 67.7 mg (content: 98 wt %) of oxalic acid was added and stirred for 17 hrs and 50 min at room temperature. The resulting slurry was filtered under suction, washed with 2 mL of ethyl acetate, and dried under reduced pressure at room temperature. 217.0 mg of the resulting colorless powder (229.1 mg obtained) was suspended in 2.5 mL of ethyl acetate, and stirred at room temperature for 15.5 hrs. The resulting slurry was filtered under suction, washed with 2 mL of ethyl acetate, and dried under reduced pressure at room temperature to obtain 193.5 mg of (1R,2S,3R,5R,6R)-2-amino-2-cyano-3-[(3,4-dichloro benzyl)oxy]-6-fluorobicyclo[3.1.0]hexane-6-carboxamide oxalate (6d) as a colorless solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08642777B2uspto-grants-2014_02