تفاعل #3253
ord-c99b877e128f477eb3b3215ab9fd97e9
معادلة التفاعل
6-(((dimethylamino)ethyl)amino)-3-hydroxy-7H-indeno[2,1-c]quinoline-7-on
pivaloyl chloride
water
→
title compound
المردود 83.8%
6-(((dimethylamino)ethyl)amino)-3-(pivaloyloxy)-7H-indeno[2,1-c]quinoline-7-on
المردود 83.8%
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1غسيلto wash the organic layer, which
- 2تجفيفwas dried over magnesium sulfate
- 3أخرىevaporated
- 4أخرىThe residue was purified by silica gel column chromatography (eluent; chloroform:ethanol=10:1(v/v)) and
- 5أخرىcrystallized from hexane
الإجراء التجريبي
To a solution of 6-(((dimethylamino)ethyl)amino)-3-hydroxy-7H-indeno[2,1-c]quinoline-7-on obtained in example 3 (100 mg, 0.3 mmol) in dichloromethane (10 ml) was added 4-dimethylaminopyridine (100 mg, 0.8 mmol) and pivaloyl chloride (37 μl, 0.3 mmol), and the mixture was stirred at room temperature for 3 hours. To the reaction mixture was added water to wash the organic layer, which was dried over magnesium sulfate and evaporated. The residue was purified by silica gel column chromatography (eluent; chloroform:ethanol=10:1(v/v)) and crystallized from hexane to give 105 mg (yield: 80.0%) of title compound. The physicochemical properties thereof are shown in table 1.