تفاعل #68077

ord-a8493697af894fe89af4b1b586e2a126

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added
  2. 2
    درجة الحرارةrefluxed
  3. 3
    درجة الحرارةwith heating for 2 hours
  4. 4
    درجة الحرارةrefluxed
  5. 5
    درجة الحرارةwith heating for 5 hours
  6. 6
    workup.WAITAfter left
  7. 7
    أخرىthe solvent was removed under reduced pressure, water
  8. 8
    workup.ADDITIONwas added
  9. 9
    أخرىThe solvent was removed under reduced pressure
  10. 10
    أخرىthe residue thus obtained
  11. 11
    أخرىwas purified by reversed-phase silica gel column chromatography [eluent; acetonitrile: water=3: 7]

الإجراء التجريبي

To 1 mL of an ethanol solution containing 0.10 g of ethyl 1-(2,3-dihydro-1,4-benzodioxin-6-ylmethyl)-4-(3-(7-methoxy-2-oxoquinolin-1(2H)-yl)propyl)piperidine-4-carboxylate, 0.15 mL of 20% aqueous sodium hydroxide solution was added and refluxed with heating for 2 hours. Then, more 0.10 mL of 20% aqueous sodium hydroxide solution was added and refluxed with heating for 5 hours. After left to stand at room temperature overnight, the solvent was removed under reduced pressure, water was added, and adjusted to pH 6.7 with 6.0 mol/L hydrochloric acid. The solvent was removed under reduced pressure, and the residue thus obtained was purified by reversed-phase silica gel column chromatography [eluent; acetonitrile: water=3: 7] to give 21 mg of 1-(2,3-dihydro-1,4-benzodioxin-6-ylmethyl)-4-(3-(7-methoxy-2-oxoquinolin-1(2H)-yl)propyl)piperidine-4-carboxylic acid as a white solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08524738B2uspto-grants-2013_09