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两相法合成4-苯基-6-甲基-5-乙氧羰基-3,4-二氢嘧啶-2(H)-酮 被引量:6

Synthesis of 4-Phenyl-6-methyl-5-ethoxycarbonyl-3,4-dihydropyrimidin-2(H)-one Using a Two-phase Method
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摘要 研究水作溶剂,三氯乙酸催化苯甲醛、乙酰乙酸乙酯、尿素在两相中缩合生成4-苯基-6-甲基-5-乙氧羰基-3,4-二氢嘧啶-2(H)-酮。最优工艺:n(苯甲醛25mmol)∶n(乙酰乙酸乙酯)∶n(尿素)=1.0∶1.5∶1.6,三氯乙酸3.0g,水7mL,无水乙醇3mL,反应温度60°C,反应时间4h,在此条件下产物的收率为91.6%。溶剂可重复使用。 The synthesis of 4-phenyl-6-methyl-5-ethoxycarbonyl-3,4-dihydropyrimidin-2 (H)-one by cyclocondensation of benzaldehyde, ethyl acetoacetate and urea in aqueous phase and in organic phase using trichloroacetic acid as catalyst and water as solvent was studied. The optimum conditions were as follows. n(benzaldehyde 25 mmol): n(ethyl acetoacetete) : n(urea)=1.0 : 1.5 : 1.6; amount of trichloroacetic acid, 3.0 g; volume of water, 7 mL; volume of absolute alcohol, 3 mL; reaction temperature, 60℃ reaction time, 4 h. The yield of the product was up to 91.6% under the above conditions. The solvent could be reused.
出处 《化学世界》 CAS CSCD 北大核心 2008年第8期487-489,480,共4页 Chemical World
关键词 BIGINELLI反应 3 4-二氢嘧啶-2(H)-酮 两相法 三氯乙酸 合成 Biginelli reaction 3,4-dihydropyrimidin-2 ( H)-one two-phase method trichloroacetic acid synthesis
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  • 1Kappe C O. 100 years of the Biginelli dihydropyrimidine synthesis [J]. Tetrahedron, 1993, 49 (32) : 6937-6963.
  • 2Rovnyak G C, Atwal K S, Hedberg A, et al. Dihydropyrimidine calcium channel blockers. 4 basic3-substituted-4-aryl-1, 4-dihydropyrimidine-5- carboxylic acid esters. Potent antihypertensive agents [J]. J Med Chem, 1992,35(17):3254-3263.
  • 3Kovnyax G C, Kimball S D, Beyer B, et al. Calcium entry blockers and activators: Conformational and structural determinants of dihydropyfimidine calcium channel modulators [J]. J Med Chem, 1995,38(1): 119-129.
  • 4Cho H, Ueda M, Shima K, et al. Dihydropyrimidines: Novel calcium antagonists with potent and long-lasting vasodilative and antihypertensive activity [J]. J Med Chem, 1989,32 (10) :2399-2406.
  • 5Wipf P, Cunningham A. A solid phase protocol of the Biginelli dihydropyrimlame synthesis suitable for combinatorial chemistry[J]. Tetrahedron Lett,1995, 36(43) :7819-7822.
  • 6Kalita H R, Phukan P. CuI as reusable catalyst for the Biginelli reaction [J]. Catal Commun, 2007, 8 (12):179-182.
  • 7彭家建,邓友全.室温离子液体催化“一锅法”合成3,4-二氢嘧啶-2-酮[J].有机化学,2002,22(1):71-72. 被引量:50
  • 8陈维一,陆军.高氯酸镁催化合成1,2,3,4-四氢嘧啶-2-酮[J].有机化学,2004,24(9):1111-1113. 被引量:14
  • 9傅南雁,袁耀锋,庞美丽,王积涛.利用三溴化铟催化的Biginelli反应原位合成3,4-二氢嘧啶-2-酮[J].高等学校化学学报,2003,24(1):79-81. 被引量:33
  • 10丁欣宇,施磊,景晓辉,朱国华,李建华,华平.HClO_4催化合成3,4-二氢嘧啶-2-酮[J].化学试剂,2007,29(3):175-176. 被引量:11

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