تفاعل #347492

ord-2851e02060cd4180856cfb554edb335e

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلwashed with 2M hydrochloric acid (2×30 ml), water, saturated NaHCO3, and brine
  2. 2
    أخرىCrude product was purified by chromatography on silica

الإجراء التجريبي

(2S,4S)-4-Acetylthio-1-allyloxycarbonyl-2-carboxypyrrolidine (1.59 g, 5.82 mM), allyl 3-aminophenoxyacetate (2.5 g, 0.012M), and 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline (3.88 g, 0.016M) were dissolved in toluene (50 ml) and stirred 18 h at ambient temperature. The reaction mixture was diluted with ethyl acetate (150 ml) and washed with 2M hydrochloric acid (2×30 ml), water, saturated NaHCO3, and brine. Crude product was purified by chromatography on silica, using a gradient from dichloromethane to dichloromethane/diethyl ether (4:1), to give title compound (3.0 g).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05527791uspto-grants-1996_06