تفاعل #164224

ord-cb4efcc83d524a708d456d499b0fb4e7

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحThe insoluble precipitate is filtered on a buckner funnel
  2. 2
    غسيلwashed with acetonitrile
  3. 3
    أخرىThe clear solution is evaporated
  4. 4
    أخرىpurified by flash chromatography (DCM/EtOH=9/1)

الإجراء التجريبي

To a solution of (R)-quinuclidin-3-yl 2-(benzylamino)-2-phenylacetate (C80) (116 mg, 0.33 mmol) in ethyl acetate (3.31 mL) and acetonitrile (3.31 mL), is added 2-bromo-1-(thiophen-3-yl)ethanone (66.5 mg, 0.32 mmol). The mixture is stirred at RT overnight. The insoluble precipitate is filtered on a buckner funnel and washed with acetonitrile. The clear solution is evaporated and purified by flash chromatography (DCM/EtOH=9/1) to obtain the title compound as a white solid (26 mg, 14% yield, bromide salt, mixture of diastereoisomers).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08835682B2uspto-grants-2014_09