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加那索酮的合成 被引量:1

Synthesis of ganaxalone
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摘要 目的:合成加那索酮。方法:以剑麻皂苷元制得的单烯醇酮醋酸酯为原料,通过6步反应合成目标化合物。结果和结论:目标物经红外光谱、核磁共振氢谱和质谱确证其化学结构,总收率达51.6%。 Objective: To synthesize ganaxalone. Methods: Ganaxalone was synthesized from pregnenolone acetate via six steps. Results: A total yield was 51.6 %. The chemical structure of the target compound was confirmed by IR, ^1H-NMR and MS. Conclusion: Ganaxalone is obtained.
出处 《中国新药杂志》 CAS CSCD 北大核心 2005年第8期1025-1026,共2页 Chinese Journal of New Drugs
关键词 加那索酮 药物合成 单烯醇酮醋酸酯 ganaxalone synthesis pregnenolone acetate
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  • 1Redely DS, Woodward R. Ganaxalone : A Prospective Overview [ J ].Drugs Fur ,2004,29(3) :227 - 242.
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  • 3Hogenkamp D J, Tahir SH, Hawkinson JE, et al. Synthesis and in vitro activity of 3β- substituted-3α-hydroxypregnan-20-ones : allosteric modulators of the GABAA receptor[J]. J Med Chem, 1997,40( 1 ) :61 - 72.
  • 4Nace HR, Nelander DH. The Application of the benzilic acid rearrangement to the synthesis of a-norpregnanes[J]. J Org Chem,1964,29(10) : 1677 - 1681.

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