반응 #6001

ord-8bde2442c4a143c2beb25e6049687eb8

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타to react at 35° to 40° C. for 3 hours
  2. 2
    workup.ADDITIONThen, the reaction mixture was poured into ice
  3. 3
    추출The mixture was extracted with diethyl ether
  4. 4
    추출the resulting extract
  5. 5
    건조was dried over anhydrous magnesium sulfate
  6. 6
    workup.DISTILLATIONThe solvent was distilled
  7. 7
    기타the thus-obtained crude crystals
  8. 8
    기타were recrystallized from diisopropyl ether/petroleum ether (1:2 by volume)

실험 절차

To 80 ml of a pyridine solution containing 10.7 g (37 mmol) of N-carbobenzoxydopamine obtained in Synthetic Example 1-(1) was added dropwise 9.9 g (93 mmol) of isobutyryl chloride at 5° to 10° C. After stirring at room temperature for 12 hours, the mixture was allowed to react at 35° to 40° C. for 3 hours. Then, the reaction mixture was poured into ice and a sodium carbonate solution and stirred at room temperature for 30 minutes. The mixture was extracted with diethyl ether and the resulting extract was dried over anhydrous magnesium sulfate. The solvent was distilled and the thus-obtained crude crystals were recrystallized from diisopropyl ether/petroleum ether (1:2 by volume) to obtain 11.9 g (yield: 74.7%) of the desired compound in the form of white cyrstals (m.p. 44°-46° C.).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05246949uspto-grants-1993_09