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Synthesis and Crystal Structure of 4-(4,6-dimethoxyl -pyrimidin-2-yl)-3-thiourea Carboxylic Acid Methyl Ester 被引量:1
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作者 HUANG Jie SONG Ji-Rong REN Ying-Hui XU Kang-Zhen MA Hai-Xia 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2006年第2期168-172,共5页
The title compound 4-(4,6-dimethoxylpyrimidin-2-yl)-3-thiourea carboxylic acid methyl ester was synthesized by the reaction of 2-amino-4,6-dimethoxyl pyrimidine, potassium thiocyanate and methyl chloroformate in eth... The title compound 4-(4,6-dimethoxylpyrimidin-2-yl)-3-thiourea carboxylic acid methyl ester was synthesized by the reaction of 2-amino-4,6-dimethoxyl pyrimidine, potassium thiocyanate and methyl chloroformate in ethyl acetate. Single crystals suitable for X-ray measurement were obtained by recrystallization with the solvent of dimethyl formamide at the room temperature. The structure was characterized by elemental analysis and IR and determined by X-ray diffraction analysis' Crystallographic data: C9H12N4O4S, Mr = 272.29, monoclinic, space group C2/m with a = 1.6672(3), b = 0.66383(12), c = 1.1617(2) nm, β = 109.275(2)°, V = 1.2136(4) nm^3, Dc = 1.490 g/cm^3,μ = 0.281 mm^-1, F(000) = 568, Z = 4, R1 = 0.0341and wR2 = 0.1042. 展开更多
关键词 4-(4 6-dimethoxylpyrimidin-2-yl)-3-thiourea carboxylic acid methyl ester synthesis X-ray diffraction
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Synthesis and Crystal Structure of 2-[(4-Methoxy- 6-methylthio-2-pyrimidinyl)aminocarbonyl- aminosulfonyl] Benzoic Acid Methyl Ester
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作者 黄明智 王晓光 +2 位作者 毛春晖 黄路 宋海斌 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2004年第7期743-746,共4页
The title compound 2-[(4-methoxy-6-methylthio-2-pyrimidinyl)aminocarbonyl- aminosulfonyl]benzoic acid methyl ester (C15H16N4O6S2, Mr = 412.44) was obtained by the reaction of (4-methoxy-6-methylthio-2-pyrimidinyl)amin... The title compound 2-[(4-methoxy-6-methylthio-2-pyrimidinyl)aminocarbonyl- aminosulfonyl]benzoic acid methyl ester (C15H16N4O6S2, Mr = 412.44) was obtained by the reaction of (4-methoxy-6-methylthio-2-pyrimidinyl)amine with 2-methoxylcarbonylbenzene-sulfonylisocya- nate. The crystal is of monoclinic, space group P21/c with a =11.169(3), b = 9.508(3), c = 17.690(5) ? b = 91.593(5), Z = 4, V = 1877.9(10) 3, Dc = 1.459 g/cm3, F(000) = 856, m(MoKa) = 0.324 mm-1, R = 0.0690 and wR = 0.1368 for 3301 observed reflections (I > 2s(I)). The N(1)H…N(3) and N(2)H…O(4) hydrogen bonds can be observed. In the molecule the phenyl plane(I), pyrimi- din-2-yl-urea bridge plane(Ⅱ) and ester plane(Ⅲ) form three conjugated systems. 展开更多
关键词 crystal structure sulfonylurea herbicide 2-[(4-methoxy-6-methylthio-2- pyrimidinyl)aminocarbonylaminosulfonyl]benzoic acid methyl ester SYNTHESIS
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防蛀剂中间体炔戊菊酯-醚化β-环糊精包合物的制备工艺
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作者 沈文 陈均志 邵超群 《陕西科技大学学报(自然科学版)》 2008年第4期61-64,共4页
通过单因素实验研究了基于饱和溶液法用醚化β-环糊精包合防蛀剂2-(硫氰基甲基硫代)苯并噻唑(TCMTB)的工艺.当醚化β-环糊精投入量为16g时,通过考察TCMTB的加入量、包合时间、包合温度、搅拌速度的影响,得到了包合物的最佳包合条件:TCMT... 通过单因素实验研究了基于饱和溶液法用醚化β-环糊精包合防蛀剂2-(硫氰基甲基硫代)苯并噻唑(TCMTB)的工艺.当醚化β-环糊精投入量为16g时,通过考察TCMTB的加入量、包合时间、包合温度、搅拌速度的影响,得到了包合物的最佳包合条件:TCMTB加入量为0.8g、包合时间为2h、包合温度为45℃、包合搅拌速度为400r/min.此条件下可获得较高的包封率产物,并对产物进行了表征. 展开更多
关键词 醚化β-环糊精 2-(硫氰基甲基硫代)苯并噻唑 包合物
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β-环糊精包合皮革防霉剂TCMTB的研究 被引量:4
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作者 陈均志 邵超群 《浙江工贸职业技术学院学报》 2009年第1期29-34,共6页
本文通过单因素实验与正交实验研究了用β-环糊精包合皮革防霉剂2-(硫氰基甲基硫代)苯并噻唑(TCMTB)的工艺。当β-环糊精投入量为4.00克时,通过改变TCMTB的加入量、包合时间、包合温度,得到作为皮革缓释长效防霉剂的最佳包合条件:TCMTB... 本文通过单因素实验与正交实验研究了用β-环糊精包合皮革防霉剂2-(硫氰基甲基硫代)苯并噻唑(TCMTB)的工艺。当β-环糊精投入量为4.00克时,通过改变TCMTB的加入量、包合时间、包合温度,得到作为皮革缓释长效防霉剂的最佳包合条件:TCMTB加入量为1.00克、包合时间为2小时、包合温度为55℃,此条件下可获得较高的包合率产物,并对产物进行了表征。应用实验表明,防霉剂包合物的防霉性能优良,且防霉时间比原药明显延长。 展开更多
关键词 Β-环糊精 2-(硫氰基甲基硫代)苯并噻唑 包合物 皮革 防霉剂
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A New Highly-Enantioselective Synthetic Process for Producing (S)-2-Hydroxybutyric Acid Methyl Ester 被引量:2
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作者 PENG Hui GUI Houying ZHOU Qiuming 《Wuhan University Journal of Natural Sciences》 CAS CSCD 2015年第4期335-342,共8页
(S)-2-aminobutyric acid being initial raw material,(S)-2-hydroxybutyric acid methyl ester was synthesized by means of a three step reaction of hydroxylation, salification and esterification. The product had a yiel... (S)-2-aminobutyric acid being initial raw material,(S)-2-hydroxybutyric acid methyl ester was synthesized by means of a three step reaction of hydroxylation, salification and esterification. The product had a yield rate of 60.4%, purity of 99% and ee value higher than 99% by characterization of GC, HPLC and 1H NMR. This synthesis technique has advantages of high purity and ee value, low cost, short reaction time and mild reaction conditions so that it is suitable for production on industrial scale. 展开更多
关键词 (S)-2-hydroxybutyric acid methyl ester (S)-2-hydroxyl butyric acid chiral drug intermediate esterification
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