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Synthesis and Crystal Structure of 1,7,7-Trimethyl- 4-(4-methoxyphenyl)-4,6,7,8-tetrahydroquinoline- 2,5(1H,3H)-diones under Microwave Irradiation
引用本文:HUA Guo-Pinga ZHU Xiao-Tongb ZHANG Jin-Pengb XU Jia-Ningb WANG Qianb JI Shun-Junc ZHANG Yongc TU Shu-Jiangb② a.Synthesis and Crystal Structure of 1,7,7-Trimethyl- 4-(4-methoxyphenyl)-4,6,7,8-tetrahydroquinoline- 2,5(1H,3H)-diones under Microwave Irradiation[J].结构化学,2006,25(5):599-603.
作者姓名:HUA  Guo-Pinga  ZHU  Xiao-Tongb  ZHANG  Jin-Pengb  XU  Jia-Ningb  WANG  Qianb  JI  Shun-Junc  ZHANG  Yongc  TU  Shu-Jiangb②  a
作者单位:HUA Guo-Pinga ZHU Xiao-Tongb ZHANG Jin-Pengb XU Jia-Ningb WANG Qianb JI Shun-Junc ZHANG Yongc TU Shu-Jiangb② a (Xuzhou Institute of Architectural Technology,Xuzhou,Jiangsu 221008,China) b (Department of Chemistry,Xuzhou Normal University,Key Laboratory of Biotechnology on Medical Plant,Xuzhou,Jiangsu 221116,China) c (College of Chemistry and Chemical Engineering,Key Laboratory of Organic Synthesis of Jiangsu Province,Suzhou University,Suzhou,Jiangsu 215006,China)
基金项目:中国科学院资助项目;江苏省自然科学基金;江苏省重点实验室基金;苏州大学校科研和校改项目
摘    要:1 INTRODUCTION Various quinolone derivatives are known to dis- play interesting biological properties ranging from microbial activity to cytotoxicity1]. They have been reported as antiviral (HIV-1)2] and antitumor agents3] as well as used as tubulin4], topoisomerase5] and thrombocyte inhibitors6]. As a member of the quino- lone family, substituted N-phenyl-2-quinolones re-present the structural basis of many biologically active compounds, such as protein kinase inhibitors, immunodu…

关 键 词:合成  晶体结构  1  7  7-三甲基-4-(4-甲氧基苯基)-4  6  7  8-四氢喹啉-2  5(1H  3H)-二酮  微波照射

Synthesis and Crystal Structure of 1,7,7-Trimethyl-4-(4-methoxyphenyl)-4,6,7,8-tetrahydroquinoline-2,5(1H,3H)-diones under Microwave Irradiation
HUA Guo-Ping,ZHU Xiao-Tong,ZHANG Jin-Peng,XU Jia-Ning,WANG Qian,JI Shun-Jun,ZHANG Yong,TU Shu-Jiang.Synthesis and Crystal Structure of 1,7,7-Trimethyl-4-(4-methoxyphenyl)-4,6,7,8-tetrahydroquinoline-2,5(1H,3H)-diones under Microwave Irradiation[J].Chinese Journal of Structural Chemistry,2006,25(5):599-603.
Authors:HUA Guo-Ping  ZHU Xiao-Tong  ZHANG Jin-Peng  XU Jia-Ning  WANG Qian  JI Shun-Jun  ZHANG Yong  TU Shu-Jiang
Institution:1. Xuzhou Institute of Architectural Technology, Xuzhou, Jiangsu 221008, China
2. Department of Chemistry, Xuzhou Normal University, Key Laboratory of Biotechnology on Medical Plant, Xuzhou, Jiangsu 221116, China
3. College of Chemistry and Chemical Engineering, Key Laboratory of Organic Synthesis of Jiangsu Province, Suzhou University, Suzhou, Jiangsu 215006, China
Abstract:The title compound (C19H23NO3) was synthesized by the one-pot reaction of p-me- thoxybenzaldehyde, Meldrum's acid, dimedone and CH3NH3Cl (NaOAc) in ethanol under micro- wave irradiation without catalyst and its crystal structure was determined by single-crystal X-ray diffraction. The crystal is of monoclinic, space group P21/c with a = 8.7462(10), b = 17.7367(19), c = 11.5959(14)(A), β = 110.981(3)°, V = 1679.6(3) (A)3, Z = 4, Dc = 1.239 g/cm3, μ(MoKα) = 0.083 mm-1, F(000) = 672 and Mr = 313.38. The structure was refined to R = 0.0530 and wR = 0.1216. X-ray analysis reveals that the dihedral angle between plane 1 (N(1), C(1), C(2), C(3)) and plane 2 (C(1), C(2), C(6), C(7), C(9)) is 3.64°, andt hat between plane 2 and plane 3 (C(11)~C(16)) is 85.33°.
Keywords:4  6  7  8-tetrahydroquinoline-2  5-diones  synthesis  microwave irradiation  crystal structure
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