期刊文献+

4-吡啶乙酸盐酸盐的合成研究

Synthesis of 2-(pyridin-4-yl)acetic Acid Hydrochloride
下载PDF
导出
摘要 介绍了标题化合物的合成方法。以4-氯吡啶盐酸盐为起始原料,先与丙二酸二乙酯反应,再用盐酸水解脱羧得到目标化合物,并经MS和1H NMR对其结构进行了表征。本合成路线原料易得、操作简便,易于实现工业化生产。反应总收率37%。 In the paper, we introduced a approach to synthetize the title compound, was realized and manufactured from 4-chloropyridine hydrochloride via tow steps. Its structure was verified by MS and 1H NMR. This synthetic route has the advantages of convenient operation and mild reaction conditions. The total product yield was 37 %. This program is suitable for industrial production.
出处 《广东化工》 CAS 2013年第18期34-34,共1页 Guangdong Chemical Industry
基金 贵州省中药现代化项目 合同编号:黔科合中药字[2010]5022号 贵州省教育厅自然科学课题 合同编号:黔教合KY字[2012]044号 贵州省高层次人才科研条件特助经费项目 合同编号:TZJF-2010年-055号
关键词 4-吡啶乙酸盐酸盐 4-氯吡啶盐酸盐 合成 2-(pyridin-4-yl)aceticacidhydroehloride 4-chloropyridinehydrochloride synthesis
  • 相关文献

参考文献6

  • 1要晓丽,崔建兰,杨玉芬.吡啶类化合物的合成及应用研究进展[J].山西化工,2012,32(1):28-31. 被引量:12
  • 2Illig Carl R,Manthey Carl L,Wall Mark J,et al.Optimization of a Potent Class of Arylamide Colony-Stimulating Factor-1 Receptor Inhibitors Leading to Anti-inflammatory Clinical Candidate 4-Cyano-N-[2-(1-cyclohexen-1-yl)-4-[1-[(dimethylamino)acetyl]-4-piperidinyl]phenyl]-1H-imidazole-2-carboxamid e (JNJ-28312141)[J].Journal of Medicinal Chemistry,2011,54(22):7860-7883.
  • 3Marion Flipo,Matthieu Desroses,Nathalie Lecat-Guillet,et al.Ethionamide Boosters:Synthesis,BiologicalActivity,and Structure-Activity Relationships of a Series of 1,2,4-Oxadiazole EthR Inhibitors[J].Journal of Medicinal Chemistry,2011,54(8):2994-3010.
  • 4Garvey David S,Holladay Mark W,Lin Nan-Homg,et al.New trisubstituted 1,2,4-triazole derivatives as potent ghrelin receptor antagonists[J].Synthesis and pharmacological in vitro and in vivo evaluations[J].Journal of MedicinalChemistry,2008,51(3):689-693.
  • 5MacLeod Angus M,Cascieri Margaret A,Merchant Kevin J,et al.Synthesis and biological evaluation of NK1 antagonists derived from L-tryptophan[J].Journal ofMedicinalChemistry,1995,38(6):934-41.
  • 6Wangke Qian,Lei Zhang,Haifeng Sun,et al.Microwave-assisted one-step synthesis of acetophenones via palladium-catalyzed regioselective arylation of vinyloxytrimethylsilane[J].Advanced Synthesis & Catalysis,2012,354(17):3231-3236.

二级参考文献16

  • 1徐兆瑜.吡啶化合物的合成技术与应用进展[J].精细化工原料及中间体,2009(2):3-8. 被引量:16
  • 2倪生良,林丹,莫勤华.氨基吡啶衍生物的合成研究进展[J].内蒙古石油化工,2006,32(10):25-27. 被引量:7
  • 3Wilson Chlarles A, Werner John A, Fujioks Georges, et al. Prepartion of (tfifluormethyl) pyridines, US: 4567273 [ P]. 1997-07-14.
  • 4Audousset M P. Hair dye compositions comprising 4,5-di- amino-l-( -hydroxy-or mehtoxyethyl) pyrazoles as oxida- tion base and 2,6-diaminopyridine as a coupling agent, EP: 1488780AI [ P]. 2004-12-22.
  • 5愈晓东.抗抑郁药奈法唑酮和曲唑酮的合成研究[D].上海:华东理工大学,2003.
  • 6Denny Williams Alexander. Preparation of pteridinones as kinnase inhibitors, WO :0119825 [ P]. 2001-05-22.
  • 7Balasubramanian Gopalan. Preparation of dibenzofuran/ dibenzothiophene derivatives useful for the treatment of inflammatory and allergic disorders, WO: 200437805 [ P]. 2004-05-06.
  • 8Knaaya N, Ishiyama T, Muto R, et al. Perparation of pyrazole carboxamide derivatives as plaetelet aggregation inhibitors for treatment of ischemia, WO: 20050673A1 [ P]. 2005-07-14.
  • 9Robertson D W, Setinbegr M I. Potassium channel modu- lators: scientific applieations and therapeutic pormise [ J ]. Journal of Medicinal Chemistry, 1900,33 ( 6 ) : 1529- 1541.
  • 10美国辉瑞有限公司.4-氨基毗啶衍生物类,CN:1032440A[P].1989-04-19.

共引文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部