تفاعل #68077
ord-a8493697af894fe89af4b1b586e2a126
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.ADDITIONwas added
- 2درجة الحرارةrefluxed
- 3درجة الحرارةwith heating for 2 hours
- 4درجة الحرارةrefluxed
- 5درجة الحرارةwith heating for 5 hours
- 6workup.WAITAfter left
- 7أخرىthe solvent was removed under reduced pressure, water
- 8workup.ADDITIONwas added
- 9أخرىThe solvent was removed under reduced pressure
- 10أخرىthe residue thus obtained
- 11أخرىwas 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.