반응 #160767

ord-d3d71713c1424731b075fa326d94fe3f

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축Upon completion, the reaction was concentrated to dryness
  2. 2
    건조The organic phase was dried with brine
  3. 3
    여과sodium sulfate, filtered
  4. 4
    농축concentrated

실험 절차

To a solution of (+/−)-tert-butyl 6-hydroxy-5-methyl-3-(3-nitropyridin-4-yl)cyclohex-2-enylcarbamate (1.0 equiv.) in pyridine (0.1M) was added Ac2O (2.0 equiv.) and the reaction was stirred at room temperature overnight. Upon completion, the reaction was concentrated to dryness, then worked-up with ethyl acetate and water. The organic phase was dried with brine, then sodium sulfate, filtered, and concentrated to give (+/−)-2-(tert-butoxycarbonylamino)-6-methyl-4-(3-nitropyridin-4-yl)cyclohex-3-enyl acetate in 94% yield. LC/MS=392.2 (M+H), Rt=0.94 min.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08829193B2uspto-grants-2014_09