The synthetic processes were discussed and the products were obtained in 80.2% yield. The reaction of 6-hydroxy-2(lH)-quinolinone were studied.
合成出6-羟基-2(1H)-喹啉酮母体，探讨了反应的机理，并对母体合成的工艺路线进行探索，讨论了各种条件对收率的影响，最后以80.2％的收率得到了6-羟基-2(1H)-喹啉酮。
参考来源 - 强心药Toborinone及6·2,447,543篇论文数据，部分数据来源于NoteExpress
Oxyquinoline and methyl-2(1H)-quinolinone were the intermediate degradation products of quinoline and methyl quinoline respectively.
喹啉和甲基喹啉的降解可生成羟基喹啉和甲基2（1H）喹啉酮中间产物。
AIM To design and synthesize 7-hydroxy-3-(substituted) phenyl-4(1H) quinolinone and 5-hydroxy-3-(substituted) phenyl-4(1H) quinolinone and to study the antiosteoporosis activity of these compounds.
目的设计并合成7 羟基3 （取代）苯基4 （1H）喹啉酮化合物及其相应的5 羟基3 （取代）苯基4 （1H）喹啉酮化合物并考察其抗骨质疏松活性。
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