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氨甲基吡嗪的制备新方法 被引量:2

A New Method for Preparation of Aminomethylpyrazine
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摘要 目的:以氰基吡嗪为原料制备氨甲基吡嗪。方法:用红铝作为还原剂还原氰基吡嗪制备氨甲基吡嗪。结果:得到了较优的反应条件:氰基吡嗪与红铝的摩尔量配比为1∶2,反应温度为0℃,反应时间为2小时。氨甲基吡嗪的收率为38%,反应条件温和。结论:本方法操作简便,还原程度可控,后处理方便。 Objective: To study the synthesis of aminomethylpyrazine starting from cyanopyrazine. Methods:Aminomethylpyrazine was prepared via reduction of cyanopyrazine by using red-Al (Trade Name: Ester,^TM solution ,70% red-Al in toluene) as reducing agent. Results:The better reaction conditions were optimized as follows: the mole ratio of cyanopyrazine to red-Al was 1:2, and the reaction temperature was 0℃, the yield of aminomethylpyrazine was 38 %. The reaction was carried out under moderate conditions. Conclusion:The process is easily handled and the degree of reduction can be controlled.
出处 《药学进展》 CAS 2007年第6期277-279,共3页 Progress in Pharmaceutical Sciences
关键词 氨甲基吡嗪 氰基吡嗪 还原 红铝 Aminomethylpyrazine Cyanopyrazine Reduction Red- Al
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参考文献8

  • 1Gribble A,Derrick I,Robert J.(Pyridylaminoalkylamino)thiadiazoles as histamine H1 antagonists:EP,194746[P].1986-09-17.
  • 2Kuramochi Takahiro,Kakefuda Akio,Yamada Hiroyoshi,et al.Synthesis and structure-activity relationships of benzyloxyphenyl derivatives as a novel class of NCX inhibitors:effects on heart failure[J].Bioorg & Med Chem,2005,13(3):725-734.
  • 3Yamada A,Tomishima M,Hayashida H,et al.Preparation of N-heterocyclyl amide compounds as 5-HT antagonists:WO,0168585A1[P].2001-09-20.
  • 4Fuchigami T,Wakasa N.Preparation of aminomethylpyrazine by hydrogenation of cyanopyrazine:JP,2001089459[P],1999-09-21.
  • 5Takamizawa Satoshi,Wakasa Noriko,Fuchikami Takamasa.Supported nickel-catalyzed hydrogenation of aromatic nitriles under low pressure conditions[J].Synlett,2001,10:1623-1625.
  • 6Hirschberg A,Mattner P G.Preparation and properties of a nitrogen mustard derived from methylpyrazine[J].J Med Chem,1968,11(4):911-912.
  • 7Hanamoto Takeshi,Fuchikami Takamasa.Remarkable dependency of diastereoselectivity on the selection of hydride sources and Lewis acids in the reduction of 2-(trifluoro-methyl) propiophenone[J].J Org Chem,1990,55(16):4696-4971.
  • 8Pei X F,Bi S.Reduction of oxindoles with sodium bis(2-methoxyethoxy)aluminum hydride,a novel reducing agent[J].Heterocycles,1994,39(1):357-360.

同被引文献15

  • 1葛欣.气相氨氧化2-甲基吡嗪制备2-氰基吡嗪研究进展[J].化学通报,2004,67(7):477-481. 被引量:2
  • 2郑杰,赵贵财,陈欣.2-甲基吡嗪的合成工艺改进[J].中国计量学院学报,2005,16(4):325-327. 被引量:1
  • 3张思晨,邱明建.新型高效还原剂红铝[J].精细与专用化学品,2006,14(3):13-15. 被引量:6
  • 4Gibble A, Derrick I ,Robert J. (Pyridylanminoalkylanmino) thiadiazoles as histamine HI antagonists [P].EP: 194 746,1986-09-17.
  • 5Kuramochi Takahiro, Kakefuda Akio, Yamada Hiroyoshi, et al. Synthesis and structure activity relationships of benzyloxyphenyl derivatives as a novel class of NCX inhibitors:effects on heart failure [J]. Bioorg & Med. Chem ,2005.13(3):725-734.
  • 6Takamizawa Sato shi, Wakasa Noriko, Fuchikami Takamasm Supported nickel catalyzed hydrogenation of aromatic nitriles under low pressure conditions [J].Synlett, 2001,10:1 623-1 625.
  • 7Mosher H S, Tessier J E. Heterocyclic basic compounds XIV: 4-phenyl-4-(3-pyridyl)-6-dimethylamino-3-hexane[J]. Journal of the American Chemistry Society, 1951, 73: 4925-4927.
  • 8Mangia Alberto, Grisenti Paride. Process tbr the preparation of alkyl mercap to methyl ergoline derivatives: DE, 3129651 [P]. 1983-02-17.
  • 9Liren Jin, Baoli Liu, Xiaojun Shi, et al. Heterocyclic carboxylie ester reducing process: CN, 1223588C [P]. 2005-10-19.
  • 10CernyZ, Fusek J, et al. Alkoxohydridoaluminates: multinuclear NMR study of sodium hydrido-(2-methoxyethoxo) aluminates[J] . Journal of OrganometallicChemistry, 1996, 516: 115-122.

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