期刊文献+

氟两相体系中2-正丙基-4-甲基-6-甲氧羰基苯并咪唑的合成 被引量:1

Synthesis of 2-(n-Propyl)-4-methyl-6-methoxycarbonylbenzimidazole in Fluorous Biphasic System (FBS)
下载PDF
导出
摘要 2-正丙基-4-甲基-6-甲氧羰基苯并咪唑是合成替米沙坦药物的重要中间体。在氟两相体系中,在不用乙酸的条件下,3-甲基-4-丁酰氨基-5-氨基苯甲酸甲酯以高产率转化为2-正丙基-4-甲基-6-甲氧羰基苯并咪唑。考察了催化剂种类及用量、全氟溶剂、反应温度和氟相循环使用对缩合反应的影响。结果表明,全氟辛基磺酸镱〔Yb(OPf)3〕和全氟萘烷(C10F18)分别是最好的催化剂和氟溶剂。在x〔Yb(OPf)3〕=0.3%,反应温度80℃,反应时间2 h的条件下,2-正丙基-4-甲基-6-甲氧羰基苯并咪唑产率为94%。含有催化剂的氟相通过简单的相分离,就可回收利用。19FNMR、GC-MS和UV-Vis检测结果显示没有催化剂或氟溶剂的损失。含有催化剂的氟相的UV-Vis光谱图分析说明,Yb(OPf)3在使用前后活性没有变化。原子发射光谱(ICP)显示,催化剂被完全(99.9%)回收,氟相重复使用10次,缩合产率从94%降至90%。 2-(n-Propyl) 4-methyl-6-methoxycarbonylbenzimidazole ( Ⅰ ) is an important intermediate of telmisartan pharmaceutical. Methyl 3-methyl4-butyrylamino-5-aminobenzoate was efficiently converted into Ⅰ in fluorous biphasic system (FBS) without acetic acid. It was found that Yb(OPf)3 and C10F18 were the best catalyst and fluorous solvent respectively for the reaction. Yield of I could be up to 94% at 80 ℃ for 2 h with x[ Yb(OPf) 3 ] = 0. 3%. By simple phase separation,the fluorous phase containing only the catalyst could be directly reused next time. Based on 19F NMR and UV - Vis and GC - MS data, no loss of catalyst or fluorous solvent to the organic phase can be detected, and no organic compounds can be found in the fluorous phase. There is no significant difference between the UV - Vis spectra of the initial and recovered fluorous phases, indicating that Yb( OPf)3 is recovered unaltered after the condensation reaction. The catalyst was completely ( 〉 99% ) recovered as determined by atomic emission spectrometry. The fluorous phase containing only catalyst can be reused up to ten times with only a slight decrease in yields from 94% to 90%.
作者 陶锋 易文斌
出处 《精细化工》 EI CAS CSCD 北大核心 2007年第8期809-812,共4页 Fine Chemicals
基金 中国博士后科学基金(20060400942)~~
关键词 2-正丙基-4-甲基-6-甲氧羰基苯并咪唑 替米沙坦 氟两相体系 全氟溶剂 全氟辛基磺酸镱 药物中间体 2-( n-propyl ) -4-methyl-6-methoxycarbonylbenzimidazole telmisartan fluorous biphasic system perfluorocarbon ytterbium perfluorooctanesulfonate drug intermediates
  • 相关文献

参考文献13

  • 1Horvath T H,Rabai J.Facile catalyst separation without water:fluorous biphase hydroformylation of olefins[J].Science,1994,266(7):72-73. 被引量:1
  • 2Cornils B,Herrmann W A.Aqueous-phase organometallic catalysis[M].New York:Wiley-VCH,1998.p.208. 被引量:1
  • 3Hanson B E.New directions in water soluble homogeneous catalysis[J].Coord.Chem Rev.,1999,185-186:795-807. 被引量:1
  • 4Yi W B,Cai C.Rare earth(Ⅲ) perfluorooctanesulfonates catalyzed Friedel-Crafts alkylation in fluorous biphase system[J].J.Fluorine Chem.,2005,126(5):831-833. 被引量:1
  • 5Yi W B,Cai C.Rare earth (Ⅲ) perfluorooctanesulfonates and perfluorooctanesulfonic acid in fluorous solvents:novel and recyclable catalytic systems for Friedel-Crafts acylation of unactivated benzenes[J].J.Fluorine Chem.,2005,126(8):1191-1195. 被引量:1
  • 6Yi W B,Cai C.Aldol condensations of aldehydes and ketones catalyzed by rare earth (Ⅲ) perfluorooctanesulfonates in fluorous solvents[J].J Fluorine Chem,2005,126(11):1553-1558. 被引量:1
  • 7Yi W B,Cai C.Mannich-type reactions of aromatic aldehydes,anilines,and methyl ketones in fluorous biphase systems created by rare earth (Ⅲ) perfluorooctanesulfonates catalysts in fluorous media[J].J Fluorine Chem,2006,127(11):1515-1521. 被引量:1
  • 8Yi W B,Cai C.Highly efficient dinitration of aromatic compounds in fluorous media using ytterbium perfluorooctanesulfonate and perfluorooctanesulfonic acid as catalysts[J].Synth Commun.2006,36(20):2957-2961. 被引量:1
  • 9Yi W B,Cai C.Cobalt(Π) perfluorooctanesulfonate catalyzed highly efficient aerobic oxidation of alcohols in fluorous biphasic systems[J].Aust J Chem,2006,59(5):349-353. 被引量:1
  • 10易文斌,蔡春.全氟辛基磺酸稀土金属盐催化氟两相酯化反应[J].有机化学,2005,25(11):1434-1436. 被引量:5

二级参考文献20

  • 1沈金龙.血管紧张素Ⅱ受体阻滞剂Telmisartan[J].药学进展,1999,23(2):121-121. 被引量:4
  • 2Beaz, G. In Comprehensive Organic Synthesis, Vol. 6,Ed.: Trost, B. M., Pergamon, Oxford, 1991, p. 323. 被引量:1
  • 3Larock, R. C. Comprehensive Organic Transformations,VCH, New York, 1989, p. 966. 被引量:1
  • 4Hah anmoto, H.; Sugimoto, Y. Bull. Chem. Soc. Jpn. 1997,70, 1421. 被引量:1
  • 5Shi, M.; Cui, S.-C. Chem. Commun. 2002, 994. 被引量:1
  • 6Nakanob, H.; Kitazume, T. Green Chem. 1999, 1, 179. 被引量:1
  • 7Shi, M.;Cui, S.-C.J. FluorineChem. 2002,116, 143. 被引量:1
  • 8Kobayashi, S.; Ishitani, H.; Nagayama, S. Synthesis 1995,1195. 被引量:1
  • 9Horvath, T. H.; Rabai, J. Science 1994, 266, 72. 被引量:1
  • 10Huhges, R. P.; Trujillo, H. A. Organometllics 1996, 15,286. 被引量:1

共引文献15

同被引文献29

  • 1Al-Harbi B G,Al-Dahlan M N,Khaldi M H. Aluminum and ironprecipitation during sandstone acidizing using organic-HF acids[C]/ /SPE International Symposium and Exhibition on FormationDamage Control,February 15 - 17,2012,Lafayette,Louisiana,USA. SPE - 151781 - MS. 被引量:1
  • 2Sopngwi J S,Gauthreaux A,Kiburz D E,et al. Successfulapplication of a differentiated chelant-based hydrofluoric acid forthe removal of aluminosilicates,fines,and scale in offshorereservoirs of the gulf of Mexico[C]//SPE International Symposiumand Exhibition on Formation Damage Control,February 26 - 28,2014,Lafayette,Louisiana,USA. SPE - 168171 - MS. 被引量:1
  • 3Gdanski R D. Kinetics of the primary reaction of HF on alumino -silicates[J].SPE Production & Facilities,2000,15 ( 4 ) : 279 -287. 被引量:1
  • 4Gdanski R D. Kinetics of the secondary reaction of HF on alumino- silicates[J].SPE Production & Facilities,1999,14 ( 4 ) : 260 -268. 被引量:1
  • 5Gdanski R. Kinetics of Tertiary reactions of hydrofluoric acid onaluminosilicates[J].SPE Production & Facilities,1998,13 ( 2 ) :75 - 80. 被引量:1
  • 6Di L,Rae P. A new acid for true stimulation of sandstonereserviores[C]//SPE Asia Pacific Oil and Gas Conference,October 28 - 31,1996,Adelaide,Australia. SPE - 37015 - MS. 被引量:1
  • 7Nasr - El - Din H A. New mechanisms of formation damage: labstudies and case histories[C]//SPE European Formation DamageConference,13 - 14May,2003,The Hague,Netherlands. SPE -82253 - MS. 被引量:1
  • 8Yang Jing( 杨静) ,Wen Xiao( 温晓) ,Ji Chaofeng( 纪朝凤) ,etal. Application of multi-hydrogen acid system on thedepressurization and stimulation of Duanliubo block in Dagangoilfield[J].钻采工艺 ,2008,31( S1) : 63 - 64. 被引量:1
  • 9Afolabi F,Opusunju A,Henri J,et al. Increasing production in abrownfield with heavy crude and fine problems by application ofnew HF-acid system case histories [C]//SPE InternationalSymposium and Exhibition on Formation Damage Control,13 - 15February,2008,Lafayette,Louisiana,USA. SPE - 112558 - MS. 被引量:1
  • 10Shuchart C E,Buster D C. Determination of the chemistry of HFacidizing with the use of19FNMR spectroscopy [C]//SPEInternational Symposium on Oilfield Chemistry,14 - 17 February,1995,San Antonio,Texas. SPE - 28975 - MS. 被引量:1

引证文献1

二级引证文献9

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