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机构地区:[1]CenterofDrugDiscovery,ChinaPharmaceuticalUniversity,Nanjing,Jiangsu210009,China [2]InstituteofPharmacologyandToxicologyAcademyofMilitarySciences,Beijing100850,china
出 处:《Chinese Journal of Chemistry》2002年第10期1115-1120,共6页中国化学(英文版)
基 金:ProjectsupportedbytheMajorStateBasicResearchDevelopmentProgramofChina (No.19980 5 1112 )
摘 要:A series of 2- and 5-(1,1-dimethyl-1,2,5,6-tetrahydropyridinium-3-yl)oxadiazoline iodides, which might be used as M 1 muscarinic receptor agonists, was synthesized from nicotin-aldehyde and nicotinhydrazine, respectively. Their structures were characterized by 1H NMR, IR, MS spectra and elemental analysis.A series of 2- and 5-(1,1-dimethyl-1,2,5,6-tetrahydropyridinium-3-yl)oxadiazoline iodides, which might be used as M 1 muscarinic receptor agonists, was synthesized from nicotin-aldehyde and nicotinhydrazine, respectively. Their structures were characterized by 1H NMR, IR, MS spectra and elemental analysis.
关 键 词:TETRAHYDROPYRIDINE oxadiazoline muscarinic receptor agonist synthesis
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