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1H NMR确证6-氟-5(或7)-氯-3-苯基-4-(1H)-喹啉酮衍生物的结构
引用本文:王晓莉,徐鸣夏.1H NMR确证6-氟-5(或7)-氯-3-苯基-4-(1H)-喹啉酮衍生物的结构[J].波谱学杂志,1998,15(6):543-546.
作者姓名:王晓莉  徐鸣夏
作者单位:华西医科大学药学院, 成都 610041
摘    要:作者合成了6-氟-3-(取代)苯基-4-(1H)-喹啉酮的5-氯衍生物与7-氯衍生物,二者极性差异小,难于分离,以混合物形式存在.所合成的化合物均未见文献报道,本文通过1H NMR上的化学位移、积分面积以及偶合常数确证了混合物中两组份的结构.

关 键 词:3-苯基-4-(1H)-喹啉酮  1H  NMR  心血管活性  
收稿时间:1998-07-20

THE STUDY ON 1H NMR OF 5(7)-CHLORO-6-FLURO-3-PHENYL-4-(1H)-QUINOLINONE DERIVATIVES
Wang Xiaoli,Xu Mingxia,Su Fu.THE STUDY ON 1H NMR OF 5(7)-CHLORO-6-FLURO-3-PHENYL-4-(1H)-QUINOLINONE DERIVATIVES[J].Chinese Journal of Magnetic Resonance,1998,15(6):543-546.
Authors:Wang Xiaoli  Xu Mingxia  Su Fu
Institution:School of Pharmacy, West China University of Medical Sciences, Chendu 610041
Abstract:Isoflavonoids are recognized to possess broad biological activities, such as cardiovascular, estrogenicity and so on.3-Pheny l-4(1H)-quinolinone derivatives are isosteres of isoflavonoids and they have similar spatial structures.So perhaps they can exhibit similar activities.5- Chloro-6-fluro-3-phenyl-4-(1H)-quinolinone derivatives and 7-chloro-6-fluro-3-phenyl-4- (1H)-quinolinone derivatives were desig ned and synthesized at the same time.It's difficult to separate them due to their similar polarity.Only two isomeres (4a, 4b)were separated. 1, 2, 3 were mix tures due to their similar polarity of the two corresponding isomeres.The structures were confirmed by 1H NMR and the contents of the mixtures were determined by HPLC.
Keywords:3-phenyl-4-(1H)-quinolinone  Derivatives  1H NMR  Cardiovascular activity  
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