تفاعل #412212

ord-f3efa4e37f874cebb02fd3f8e54d0e7d

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحAfter filtration through Celite the solvent
  2. 2
    أخرىwas evaporated
  3. 3
    أخرىThe residue was purified by preparative HPLC (60% CH3CN/aq:0.1M NH4OAc)

الإجراء التجريبي

A suspension of 3-[2-(4-amino{t-butoxycarbonylimino}methylphenyl)-ethoxy]nitrobenzene (1.47 g; 3.81 mmol; from step (iii) above) and Pd (0.236 g; 5% on charcoal) in EtOH (75 mL) was stirred under H2(g) (1 atm.) for 25 minutes. After filtration through Celite the solvent was evaporated. The residue was purified by preparative HPLC (60% CH3CN/aq:0.1M NH4OAc) to afford the sub-title compound. Yield: 1.02 g (75%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06221898B1uspto-grants-2001_04