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2α-和4α-唑取代-5α-雄甾-3,17-二酮的绿色合成 被引量:1

Green method for synthesis of 2α and 4α-azole-substituted-5α-androstan-3,17-dione
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摘要 表雄酮经Jones氧化、溴化得2α-溴-5α-雄甾-3,17-二酮,后者与系列唑在无溶剂熔融条件下反应得标题化合物。与溶剂法比较,该法操作简便、反应时间短、收率高,且绿色环保。 2α-Bromine-5a-androstan-3,17-dione was synthe-sized from epiandrosteronevia Jones oxidation and bromina- tion. And then the bromide reacted with azoles under solvent- free conditions to give 2a-azole-substituted-5a-androstan- 3,17- dione and 4a-azole-substituted-5a-androstan-3, 17-di- one. The method is convenient and quick with high yield and environmental friendliness.
出处 《化学试剂》 CAS CSCD 北大核心 2013年第3期271-273,共3页 Chemical Reagents
基金 国家自然科学基金资助项目(21102109) 湖北省自然科学基金资助项目(2010CDB06501) 武汉市青年科技晨光计划资助项目(201271031390) 湖北省教育厅资助项目(B20104606) 武汉市教育局资助项目(2009K103)
关键词 2α-溴-5α-雄甾-3 17-二酮 无溶剂反应 绿色合成 2α-bromine-Sa-androstan-3, 17-dione solvent- free reaction green synthesis
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参考文献13

  • 1MOREIRA V M A,VASAITIS T S,NJAR V C O,et a Synthesis and evaluation of novel 17-indazole androstel derivatives designed as CYP17 inhibitors [ J]. Steroid. 2007,72 ( 14 ) :939-948.
  • 2ZHU Na, LING Yang-zhi, LEI Xiao-ping, et al. Novel P45017a inhibitors: 17-( 2'-oxazolyl ) - and 17-( 2'-thia- zolyl) -androstene derivatives [ J ]. Steroids, 2003,68 ( 7/ 8) :603-611.
  • 3CLEMENT O O,FREEMAN C M,HARTMANN R W,et al. Three dimensional pharmacophore modeling of human CYP17 inhibitors, potential agents for prostate cancer therapy[J]. J. Med. Chem. ,2003,46(12) :2 345-2 351.
  • 4柯贤炳,胡吴,胡先明.氨基甾体神经肌肉阻断剂的研究进展,药物化学进展[M].化学工业出版社,2009:134.148.
  • 5KE Xian-bing,HU Hao,ZHANG Ke-da, et al. Significant steroids:effective and general synthesis of 4a- and 48- amino-5ct-androstanes[ J]. Chem. Commun. ,2009 : 1 037- 1 039.
  • 6Xian-bing, HU Hao,ZHOU Ding-shan,et al. A facile and general synthesis of 2-aminosteroids [ J ]. Synthesis, 2009, ( 8 ) : 1 255-1 260.
  • 7GUO Hao, ZHANG Guo-lan, ZHANG Tao, et al. Synthe- sis, characterization and biological evaluation of some16/3-azolyl-3fl-amino-5a-androstane derivatives as poten- tial anticancer agents [ J ]. Eur. J. Med. Chem. , 2011 , 46 (9) :3 662-3 674.
  • 8BARALDI P G, PRETI D, TABRIZI M A. New pyrrolo [ 2, l-f] purine-2,4-dione and imidazo [ 2, l-f] purine- 2,4-dione derivatives as potent and selective human a3 adenosine receptor antagonists J ]. J. Med. Chem. ,2005, 48(14) :4 697-4 701.
  • 9WALSH P J, LI Hong-mei, DE PARRODI C A. A green chemistry approach to asymmetric catalysis: solvent-free and highly concentrated reactions[ J]. Chem. Rev. ,2007, 107(6) :2 503-2 545.
  • 10王小利,刘明星,王贤文,苏江涛,林松.无溶剂合成α-溴-4-甲氧基苯乙酮[J].化学试剂,2011,33(4):377-378. 被引量:2

二级参考文献8

  • 1于佩凤.α-氨基苯乙酮盐酸盐和其对位取代衍生物的合成[J]化学试剂,1986(05).
  • 2KAVALA V,NAIK S,PATEL B K.A new recyclable dit-ribromide reagent for efficient bromination under solventfree condition. Journal of Organic Chemistry . 2005
  • 3Buu-HoI。Ng Ph,Xuong Ng D,KhoI。Ng H.Three new analogues of chloramphenicol. Journal of the American Chemical Society . 1951
  • 4Paul S,Gupta V,Gupta R,Loupy A.Microwave-induced selective synthesis of α-bromo and α,α-dibromoalkanones using dioxane-dibromide and silica gel under solvent-free conditions. Tetrahedron Letters . 2003
  • 5Tanaka K,Toda F.Solvent-free organic synthesis. Chemical Reviews . 2000
  • 6Rebstock MC,Pfeiffer EL.The synthesis of p -phenoxy and methoxy compounds. Journal of the American Chemical Society . 1952
  • 7苏冰,鲍亚杰,李洪军,王雅丽,李晓东.对甲氧基-α-溴代苯乙酮的合成[J].中国医药工业杂志,2001,32(8):374-374. 被引量:22
  • 8彭安顺,王立斌.用溴化铜代替液溴合成对甲氧基-α-溴代苯乙酮[J].辽宁化工,2003,32(1):17-18. 被引量:12

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