تفاعل #59752

ord-13e7cc1702f94e2989b1e4c1c9965463

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe excess triethylorthopropionate was evaporated under vacuum
  2. 2
    أخرىthe residue purified by bond-elut (silica)
  3. 3
    غسيلeluting with an ethyl acetate/cyclohexane gradient
  4. 4
    أخرىThe solvent was evaporated from the product fractions under vacuum

الإجراء التجريبي

N-Cyclopropyl-4′-(hydrazinocarbonyl)-6-methyl-1,1′-biphenyl-3-carboxamide (Intermediate 40) (50 mg) in triethylorthopropionate (5 ml) was heated at 150° C. for 18 hours. The excess triethylorthopropionate was evaporated under vacuum and the residue purified by bond-elut (silica), eluting with an ethyl acetate/cyclohexane gradient. The solvent was evaporated from the product fractions under vacuum to give N-cyclopropyl-4′-(5-ethyl-1,3,4-oxadiazol-2-yl)-6-methyl-1,1′-biphenyl-3-carboxamide.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07425555B2uspto-grants-2008_09