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N-(5-邻氯苯基-2-呋喃甲酰氨基)丙氨酰胺衍生物的合成和生物活性测定 被引量:6
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作者 胥杨 薛思佳 +3 位作者 孙晋峰 方治坤 尹安琴 陈龙 《有机化学》 SCIE CAS CSCD 北大核心 2008年第11期1997-2000,共4页
以5-邻氯苯基-2-呋喃甲酰氯和丙氨酸为起始原料,通过非均相法得到N-(5-邻氯苯基-2-呋喃甲酰氨基)丙氨酸,再与10种不同取代苯胺反应,通过N,N'-二环己基碳二亚胺和4-二甲氨基吡啶(DCC/DMAP)偶合法设计合成了10个未见文献报道的N-(5-... 以5-邻氯苯基-2-呋喃甲酰氯和丙氨酸为起始原料,通过非均相法得到N-(5-邻氯苯基-2-呋喃甲酰氨基)丙氨酸,再与10种不同取代苯胺反应,通过N,N'-二环己基碳二亚胺和4-二甲氨基吡啶(DCC/DMAP)偶合法设计合成了10个未见文献报道的N-(5-邻氯苯基-2-呋喃甲酰氨基)丙氨酰胺类衍生物4a~4j.通过元素分析,1HNMR,IR和MS确定化合物的结构,初步生物活性测试表明标题化合物具有一定的除草活性. 展开更多
关键词 丙氨酸 5-邻氯苯基-2-呋喃甲酰氯 酰胺 衍生物合成 除草活性
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1-取代哌啶-4-酮肟醚的合成与杀菌活性测定 被引量:2
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作者 尹安琴 薛思佳 +2 位作者 方治坤 陈龙 胥杨 《有机化学》 SCIE CAS CSCD 北大核心 2009年第3期454-458,共5页
以取代苄胺或苯乙胺为起始原料,依次经Michael加成,Dieckmann缩合,水解脱羧,肟化和醚化等多步反应合成了11个未见文献报道的1-取代哌啶-4-酮肟醚5a~5k.目标化合物的结构经元素分析,IR,1H NMR和MS测定确证.初步杀菌活性测试表明,部分化... 以取代苄胺或苯乙胺为起始原料,依次经Michael加成,Dieckmann缩合,水解脱羧,肟化和醚化等多步反应合成了11个未见文献报道的1-取代哌啶-4-酮肟醚5a~5k.目标化合物的结构经元素分析,IR,1H NMR和MS测定确证.初步杀菌活性测试表明,部分化合物有较好的杀菌活性. 展开更多
关键词 1-取代-4-哌啶酮 肟醚 合成 杀菌活性
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Synthesis,Crystal Structure and Herbicidal Activity of N-(4-Methylbenzyl)-4-(3-fluorophenyl)-4-piperidinol Hydrochloride 被引量:1
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作者 方治坤 薛思佳 +2 位作者 陈龙 胥杨 尹安琴 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2009年第7期841-846,共6页
A novel compound N-(4-methylbenzyl)-4-(3-fluorophenyl)-4-piperidinol hydrochloride has been synthesized and its structure (C19H23ClFNO, Mr = 335.83) was characterized by elemental analysis, IR, ^1H NMR, MS and s... A novel compound N-(4-methylbenzyl)-4-(3-fluorophenyl)-4-piperidinol hydrochloride has been synthesized and its structure (C19H23ClFNO, Mr = 335.83) was characterized by elemental analysis, IR, ^1H NMR, MS and single-crystal X-ray diffraction analyses. The crystal belongs to the triclinic system, space group P1 with a = 7.2163(6), b = 10.7905(9), c = 12.2651(10) A, α = 109.576(2),β = 98.407(2),γ= 95.956(2)°, V= 878.14(13)A3, Z = 2, Dc = 1.270 g/cm^3,μ = 0.231 mm^-1, F(000) = 356, S = 1.100, the final R = 0.0525 and wR = 0.1425 for 3206 unique reflections (Rint = 0.0140) with 2736 observed ones (I 〉 2σ(I)). The piperidine ring exhibits a chair conformation. The dihedral angle made by the methyl- and fluoro-substituted benzene rings is 66.84(7)°. There are some intra- and intermolecular hydrogen bonding interactions among the molecules, which stabilize the whole crystal structure. The preliminary biological activity tests indicate good herbicidal activity for the title compound, in particular against the roots of some tested plants (such as Brassica campestris L. and Echinochloa crusgallis L.). 展开更多
关键词 SYNTHESIS crystal structure herbicidal activity PIPERIDINOL
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Synthesis,Crystal Structure and Bioactivity of N-Phenethyl-4-hydroxy-4-phenyl Piperidine Hydrochloride 被引量:1
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作者 王海峰 薛思佳 +3 位作者 祝俊 杨定荣 金甲 方治坤 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2009年第6期742-746,共5页
A novel compound N-phenethyl-4-hydroxy-4-phenyl piperidine hydrochloride (C19H24ClNO·H2O) has been synthesized and structurally characterized by elemental analysis, IR, ^1H NMR spectra and single-crystal X-ray ... A novel compound N-phenethyl-4-hydroxy-4-phenyl piperidine hydrochloride (C19H24ClNO·H2O) has been synthesized and structurally characterized by elemental analysis, IR, ^1H NMR spectra and single-crystal X-ray diffraction. The crystal belongs to orthorhombic, space group P212121 with a = 8.6306(8), b = 11.0464(10), c = 19.3221(18)A^°, V = 1842.1(3)A^°^3, Z = 4, Dc =1.211 g/cm^3,μ = 0.217 mm^-1, Mr= 335.86, F(000) = 720, S = 0.973, R = 0.0420 and wR = 0.1009 for 3627 unique reflections with 3157 observed ones (I 〉 2σ(I)). In the crystal, the dihedral angles made by piperidine ring with two benzene rings are 84.8(6) and 62.5(7)°, respectively. Intermolecular O-H…O and O-H…Cl hydrogen bonds involving water molecules form chains along the b axis, which stabilizes the crystal structure. The preliminary bioactivity tests indicated that the title compound has good effect of cellular growth inhibition to K562 cells and potential bioactivity of anti-leukemia. 展开更多
关键词 crystal structure piperidine derivatives SYNTHESIS bioactivity
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Synthesis,Crystal Structure and Antifungal Activity of N-(Pyridine-2-methyl)-2-(4-chlorophenyl)-3-methylbutanamide
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作者 陈龙 薛思佳 +2 位作者 方治坤 尹安琴 胥杨 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2009年第8期990-994,共5页
A novel compound N-(pyridine-2-methyl)-2-(4-chlorophenyl)-3-methylbutanamide, a racemic compound, has been synthesized with 2-(4-chlorophenyl)-3-methylbutyric acid and pyridin- 2-methylanamine as the raw materia... A novel compound N-(pyridine-2-methyl)-2-(4-chlorophenyl)-3-methylbutanamide, a racemic compound, has been synthesized with 2-(4-chlorophenyl)-3-methylbutyric acid and pyridin- 2-methylanamine as the raw materials, and its crystal structure (C17H19C1N2O, Mr = 302.79) was determined by single-crystal X-ray diffraction analysis. The crystal belongs to monoclinic, space group P21/n with a = 9.624(9), b = 23.14(2), c = 15.626(15)A, β = 106.199(14)°, V = 3342(5) A^3, Z = 8, Dc = 1.204 g/cm^3,μ = 0.23 mm^-1, F(000) = 1280, S = 1.032, R = 0.0681 and wR = 0.1508 for 6513 unique reflections (Rint = 0.0421) with 3375 observed ones. In the crystal structure, there are some intermolecular hydrogen bonds which stabilize the crystal structure. The preliminary bioassay shows that the title compound exhibits good antifungal activity against Botrytis cinerea, Gibberella zeae, Dothiorella gregaria and Colletotrichum gossypii. 展开更多
关键词 2-(4-chlorophenyl)-3-methylbutyric acid crystal structure SYNTHESIS antifungaiactivity
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(S)-(+)-N-取代吡咯烷甲醇衍生物的合成及晶体结构 被引量:1
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作者 尹安琴 薛思佳 +2 位作者 方治坤 陈龙 胥杨 《有机化学》 SCIE CAS CSCD 北大核心 2010年第4期601-605,共5页
从L-α-脯氨酸出发,经过酯化、N-烷基化、与格氏试剂反应合成了6个未见文献报道的(S)-(+)-N-取代吡咯烷甲醇衍生物3a~3f,其结构经IR,1HNMR和元素分析测定确证.并用X射线单晶衍射法测定了化合物(S)-(+)-1-[N-(5-氯-2-噻唑甲基)-2-吡咯烷... 从L-α-脯氨酸出发,经过酯化、N-烷基化、与格氏试剂反应合成了6个未见文献报道的(S)-(+)-N-取代吡咯烷甲醇衍生物3a~3f,其结构经IR,1HNMR和元素分析测定确证.并用X射线单晶衍射法测定了化合物(S)-(+)-1-[N-(5-氯-2-噻唑甲基)-2-吡咯烷基]-1,1-二苯基甲醇(3e)的晶体结构.晶体为单斜晶系,空间群为P2(1),a=0.8737(14)nm,b=0.9098(14)nm,c=1.2180(17)nm,α=90.00°,β=92.55(3)°,γ=90.00°,V=0.9671(3)nm3,Z=2,Dc=1.3217g/cm3,F(000)=404,R=0.0584,wR=0.1335. 展开更多
关键词 N-取代吡咯烷甲醇 单晶结构 合成
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瑞德西韦制备工艺中手性杂质的合成
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作者 方治坤 朱阳 姚长亮 《中国医药工业杂志》 CAS CSCD 北大核心 2022年第8期1141-1147,共7页
为了增强对瑞德西韦的质量控制,设计合成了其工艺路线中易产生的重要手性杂质,包括(S)-2-[[(S)-[[(2R,3S,4R,5S)-5-(4-氨基吡咯并[2,1-f][1,2,4]三嗪-7-基)-5-氰基-3,4-二羟基四氢呋喃-2-基]甲氧基](苯氧基)磷酰基]氨基]丙酸-2-乙基丁基... 为了增强对瑞德西韦的质量控制,设计合成了其工艺路线中易产生的重要手性杂质,包括(S)-2-[[(S)-[[(2R,3S,4R,5S)-5-(4-氨基吡咯并[2,1-f][1,2,4]三嗪-7-基)-5-氰基-3,4-二羟基四氢呋喃-2-基]甲氧基](苯氧基)磷酰基]氨基]丙酸-2-乙基丁基酯,以及其(S)-2-[(R)-(2R,3S,4R,5R)]-型和(S)-2-[(R)-(2R,3S,4R,5S)]-型光学异构体,这些化合物的结构通过MS和NMR确证。本工艺条件温和、收率高、无需手性分离,适合实验室规模制备。 展开更多
关键词 瑞德西韦 新型冠状病毒肺炎 手性杂质
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