共查询到17条相似文献,搜索用时 140 毫秒
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微波催化固相法合成3,4-二氢嘧啶-2(1H)-酮 总被引:2,自引:0,他引:2
在固相无溶剂条件下,使用微波辐射技术,由β-酮酸酯、芳香醛、脲合成了一系列3,4-二氢嘧啶-2(1H)-酮,实验简单方便,产率高,纯度高。 相似文献
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以取代芳醛(1a~1h),乙酰乙酸乙酯(2)和脲(3)为原料,MMT/CuCl2为催化剂,乙醇为溶剂,在超声条件下经Beginelli反应合成了8个3,4-二氢嘧啶-2(1H)-酮衍生物(4a~4h),其结构经1H NMR和IR确证。以4a为例,分别采用单因素法和正交实验法研究了催化剂、溶剂、反应温度、超声时间和物料比r[n(1a): n(2) :n(3)]对4a产率的影响。结果表明:在最优反应条件(1a 2.4 mol, r=1.2 : 1.0 : 1.0, MMT/CuCl220 mol%, EtOH 1 mL,于90 ℃超声15 min)下,4a产率88.4%。 MMT/CuCl2循环使用3次,产率基本不变。 相似文献
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异黄酮化合物具有心血管活性[1],雌激素活性[2]及抗骨质疏松[3]活性等。3 苯基 4(1H)喹啉酮衍生物是异黄酮化合物的等电子体,文献报道它具有与异黄酮化合物相似的心血管活性[4]和抗肿瘤[5]活性。结构中具有氟原子的化合物大多能改善脂溶性,增强生理活性,且能选择性作用于脑细胞及脑血管;喹诺酮类抗菌药中具有优良抗菌活性的化合物几乎都含有氟原子。我们对含氟的3 苯基 4(1H)喹啉酮类化合物进行了研究。以氟氯苯胺为原料,合成了其7 氯衍生物(化合物A1~A4),及5 氯衍生物(化合物B1~B4),其中7 氯衍生物为主产物,合成路线如下:化合… 相似文献
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YU Chen-Xia ZHU Xiao-Tong YAO Chang-Sheng TU Shu-Jiang 《结构化学》2007,26(5):533-536
The title compound (C16H14BrNO) has been synthesized by the reaction of p-tolylamine, Meldrum’s acid and 4-bromo-benzaldehyde, and its structure was characterized by IR, 1H NMR and X-ray single-crystal diffraction. The crystal belongs to monoclinic, space group P21/n with a = 7.6850(11), b = 8.3004(11), c = 21.301(3) , β = 95.110(2)°, V = 1353.4(3) 3, Mr = 316.19, Z = 4, Dc = 1.552 g/cm3, μ(MoKα) = 3.028 mm-1, F(000) = 640, the final R = 0.0345 and wR = 0.0768. X-ray analysis reveals that the atoms of C(1), C(2), C(3), C(4), C(5) and N(1) form a six-membered ring of boat conformation. 相似文献
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Ya. Yu. Yakunin V. D. Dyachenko V. P. Litvinov 《Chemistry of Heterocyclic Compounds》2001,37(5):581-587
5-Acetyl-3-cyano-6-methylpyridine-2(1H)-thione was obtained by the reaction of ethoxymethyleneacetylacetone with cyanothioacetamide in the presence of N-methylmorpholine. Its alkylation, bromination of the 2-methylthio derivative, and the conversions of its 5-bromoacetyl derivative have been studied. 相似文献
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4-羟基-2,5-二甲基-3(2H)呋喃酮的合成 总被引:3,自引:0,他引:3
总结了食品增香剂4-羟基-2.5-二甲基-3(2H)呋喃国的合成方法,包括近期的合成研究进展,对一些合成方法的优缺点作了评述。参考文献28篇。 相似文献
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The Synthesis of 3-(2'-Hydroxybutyl) isobenzofuran-1 (3H)-one 总被引:1,自引:0,他引:1
l(3H】.Isobenzoturans(Dhthalldes】werereDortedtoexhibitawiderangeofbiologicalactivities.Forexample,3-n-butylphthallde(NB)exhibitsantlasthmatlc’,antlconvuls-ant“actlvltles.PenEandZhouhavestudiedonthemetabolismofNBPInrats‘.Theyfoundthat... 相似文献
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2-Substituted-2,3-dihydro-4(1H)-quinazolinones were synthesized in high yield by condensation of 2-anthranilamide with aromatic aldehydes or ketones in refluxing water without catalyst.This protocol has advantages of high yield,simple work-up and environmental friendly procedure. 相似文献
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A new method is proposed for the synthesis of 2-amino-4(5H)-oxothiophenes with aryl and hetaryl substituents in position 3 of the molecule by the acylation of aryl- and 2-azahetarylacetonitriles with mercaptoacetic acid ethyl ester.__________Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 202–205, February, 2005. 相似文献
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Xin Ming Zhou Zhi Bing Zheng Hong Ying Liu Wu Zhong Jun Hai Xiao Li Li Wang Song Li 《中国化学快报》2007,18(8):905-908
A new series of compounds,1-aryl-3-(3,4-dihydro-2H-chromen-5-yl) ureas,have been synthesized and their structures were confirmed by FAB-MS and ~1H NMR.The preliminary pharmacological screening showed that these compounds inhibited TNF-αproduction in lipopolysaccharide (LPS)-stimulated THP-1 cells. 相似文献