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Novel synthesis of 2-butyl-5-chloro-3H-imidazole-4-carbaldehyde:A key intermediate of Losartan 被引量:3
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作者 Hai Bo Sun Guo Jun Zheng +2 位作者 Ya Ping Wang Xiang Jing Wang Wen Sheng Xiang 《Chinese Chemical Letters》 SCIE CAS CSCD 2009年第3期269-270,共2页
A novel method for synthesis of 2-butyl-5 -chloro-3H-imidazole-4-carbaldehyde 2, a key intermediate of Losartan was reported. The compound 2 was synthesized from starting material dimethyl malonate 6 and n-valeronitri... A novel method for synthesis of 2-butyl-5 -chloro-3H-imidazole-4-carbaldehyde 2, a key intermediate of Losartan was reported. The compound 2 was synthesized from starting material dimethyl malonate 6 and n-valeronitrile 8 by six steps with an overall yield of 40%. The key step including the reaction of compound 5 with POCl3/DMF followed by hydrolysis to give compound 2 with the yield of 68%. 展开更多
关键词 LOSARTAN ANTIHYPERTENSIVE Angiotensin II 2-Butyl-5-chloro-3H-imidazole-4-carbaldehyde
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Stereoselective Synthesis of 2-Chloro-4-Substituted-phenyl-5,5-Dimethyl-1,3,2-Dioxaphosphorinan-2-(Thi)ones 被引量:1
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作者 Rui Lian SHAO Guang Fu YANG +1 位作者 Wei Shi MIAO Min Hua YANG(National Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin, 300071) 《Chinese Chemical Letters》 SCIE CAS CSCD 1997年第10期855-858,共4页
The stereoselective synthesis of 2-chloro-4-substituted-phenyl-5,5-dimethyl-1,3,2-dioxaphosphorinan-2-(thi)ones is described. Only single trans-isomers were obtained when 1-substituted-phenyl-2,2-dimethyl-1,3-propaned... The stereoselective synthesis of 2-chloro-4-substituted-phenyl-5,5-dimethyl-1,3,2-dioxaphosphorinan-2-(thi)ones is described. Only single trans-isomers were obtained when 1-substituted-phenyl-2,2-dimethyl-1,3-propanediols (1) reacted with POCl3. But the stereoselectivity of cyclization reaction between (1) and PSCl3 depended greatly upon the reaction condition. The configurational assignments and the ratio of cis-/trans- diastereoisomers of the products were performed on the basis of (HNMR)-H-1, (PNMR)-P-31 and IR spectra and confirmed by X-ray diffraction analyses. 展开更多
关键词 HNMR Cl Stereoselective Synthesis of 2-chloro-4-Substituted-phenyl-5 5-Dimethyl-1 3 2-Dioxaphosphorinan-2 Thi)ones
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Single-crystal Cultivation and Structure Analysis of Unstable 1-Azido-2-chloro-4-nitrobenzene
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作者 程小波 成昌梅 +1 位作者 王如骥 郝戬 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2014年第12期1801-1806,共6页
The 1-azido-2-chloro-4-nitrobenzene was prepared by nucleophilic substitution between 2-chloro-4-nitro-1-(trifluoromethylsulfinyl)benzene and sodium azide, and its structure was characterized by NMR spectrum and X-ray... The 1-azido-2-chloro-4-nitrobenzene was prepared by nucleophilic substitution between 2-chloro-4-nitro-1-(trifluoromethylsulfinyl)benzene and sodium azide, and its structure was characterized by NMR spectrum and X-ray single-crystal diffraction. It crystallizes in the monoclinic system, space group P21/n, Z = 8 and Mr = 198.57. A cultivation process of the single crystal of unstable aryl azide was provided. The group of trifluoromethyl sulfinyl was found for the first time to be a new excellent leaving group of aromatic nucleophilic substitution reactions. 展开更多
关键词 1-azido-2-chloro-4-nitrobenzene aromatic nucleophilic substitution X-ray single-crystal diffraction trifluoromethylsulfinyl
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Synthesis,Crystal Structure and Anti-tumor Activity of 2-(2-Chloro-4-nitrophenyl)-4-(4-chlorophenyl)-3a,4-diethoxy-2,3,3a,4-tetrahydrochromeno[3,4-d][1,2,3]diazaphosphole
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作者 应华洲 孙茂堂 +1 位作者 刘滔 胡永洲 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2008年第10期1171-1174,共4页
The title compound 2-(2-chloro-4-nitrophenyl)-4-(4-chlorophenyl)-3a,4- diethoxy- 2,3,3a, 4-tetrahydrochromeno[3,4-d][1,2,3]diazaphosphole 2 (C29H30Cl2N3O7P, Mr = 633.44) was synthesized and its structure was cha... The title compound 2-(2-chloro-4-nitrophenyl)-4-(4-chlorophenyl)-3a,4- diethoxy- 2,3,3a, 4-tetrahydrochromeno[3,4-d][1,2,3]diazaphosphole 2 (C29H30Cl2N3O7P, Mr = 633.44) was synthesized and its structure was characterized by IR, MS, ^1H NMR, ^13C NMR, ^31p NMR, elemental analysis and single-crystal X-ray diffraction. It crystallizes in triclinic, space group P1^-, a = 9.1549(3), b = 10.7168(4), c = 17.6272(6)A, α = 102.9363(12), β = 90.2713(9), γ = 117.4265(10)°, V= 1484.41(9)A^3, Z= 2,μ(MoKa) = 0.323, F(000) = 658, Z= 2, De= 1.417 g/cm^3, the final R = 0.0687 and wR = 0.2066 for 4943 observed reflections (I 〉 2σ(I)). X-ray analysis reveals that the diazaphospholine ring is almost planar and the two ethoxy groups bonded on the 3a- and 4-positions are in trans configurations. Its antiproliferative activity was also tested in vitro against four human tumor cell lines. 展开更多
关键词 SYNTHESIS crystal structure 2-(2-chloro-4-nitrophenyl)-4-(4-chlorophenyl)-3a 4-diethoxy-2 3 3a 4-tetrahydrochromeno[3 4-d] [1 2 3]dlazaphosphole ANTITUMOR
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(Z)-N-(3-(2-Chloro-4-nitrophenyl)-4-methylthiazol-2(3H)-ylidene) Pivalamide: Synthesis and Crystal Structure
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作者 Aamer Saeed Michael Bolte 《Journal of Crystallization Process and Technology》 2011年第3期41-48,共8页
Synthesis of the title compound was carried out by base-catalyzed cyclization of 1-pivaloyl-3-(2-chloro-4-nitrophenyl) thiourea with α-bromoacetone produced in situ. The structure was confirmed by the spectroscopic a... Synthesis of the title compound was carried out by base-catalyzed cyclization of 1-pivaloyl-3-(2-chloro-4-nitrophenyl) thiourea with α-bromoacetone produced in situ. The structure was confirmed by the spectroscopic and elemental analysis and single crystal X-ray diffraction data. It crystallizes in the triclinic space group P-1 with unit cell dime sions a = 8.7137(10), b = 10.2010(14), c = 10.6593(13), α = 62.671(9), β = 82.701(10), γ = 79.762(10), V = 827.21(8) ?3, Z = 2. 展开更多
关键词 SYNTHESIS 1-Pivaloyl-3-(2-chloro-4-nitrophenyl) THIOUREA (Z)-N-(3-(2-chloro-4-nitrophenyl)-4-methylthiazol-2(3H)-ylidene) Pivalamide CRYSTAL Structure
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4-氯-5-硝基-2-氨基苯酚的合成
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作者 吴小平 宋健 +2 位作者 冯荣秀 周雪娟 陈磊 《染料工业》 2002年第6期30-31,29,共3页
本文以4-氯-2-氨基苯酚为起始原料合成了4-氯-5-硝基-2-氨基苯酚。4-氯-2-氨基苯酚经醋酐酰化制得2-乙酰氨基-4-氯苯酚,粗产率为92.4%,熔点为170.3℃~171 3℃。然后分别以氯苯,邻二氯苯为脱水剂在回流条件下反应15小时,经真空蒸馏得... 本文以4-氯-2-氨基苯酚为起始原料合成了4-氯-5-硝基-2-氨基苯酚。4-氯-2-氨基苯酚经醋酐酰化制得2-乙酰氨基-4-氯苯酚,粗产率为92.4%,熔点为170.3℃~171 3℃。然后分别以氯苯,邻二氯苯为脱水剂在回流条件下反应15小时,经真空蒸馏得到5-氯-2-甲基苯并(?) 唑,熔点为52℃-54℃。将5-氯-2-甲基苯并(?)唑进行硝化反应,得到5-氯-6-硝基-2-甲基苯并(?)唑,粗产率84.76%,熔点为135.5℃-139.0℃。5-氯-6-硝基-2-甲基苯并(?)唑在强碱条件下水解后,经酸析得到4-氯-5-硝基-2-氨基苯酚,粗产率为90.10%.熔点为209.8~210.0℃。 展开更多
关键词 4-氯-5-硝基-2-氨基苯酚 合成 2-乙酰氨基-4-氯苯酚 5-氯-2-甲基苯并恶唑 5-氯-6-硝基-2-甲基苯并恶唑
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Crystal Structure and Biological Activities of (R)-N′-[2-(4-Methoxy-6-chloro)-pyrimidinyl]-N-[3-methyl-2-(4-chlorophenyl)butyryl]-urea
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作者 LI Jing-Zhi XUE Si-Jia LIU Guo-Hua 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2006年第8期903-908,共6页
The title compound (R)-N′-[2-(4-methoxy-6-chloro)-pyrimidyl]-N-[3-methyl-2-(4- chlorophenyl)butyryl]-urea has been synthesized, and its crystal structure and biological behaviors were studied. Crystallographic ... The title compound (R)-N′-[2-(4-methoxy-6-chloro)-pyrimidyl]-N-[3-methyl-2-(4- chlorophenyl)butyryl]-urea has been synthesized, and its crystal structure and biological behaviors were studied. Crystallographic data: C17H18C12N4O3, Mr = 397.25, monoclinic, space group P21/c, a = 12.331(2), b = 14.025(3), c = 23.085(5) A, β = 99.607(4)°, Z = 8, V = 3936.2(13) A3, Dc = 1.341 g/cm^3, F(000) = 1648, R = 0.0718, wR = 0.1585 and/t(MoKα) = 0.353 mm^-1. The preliminary biological tests showed that the title compound has definite insecticidal and fungicidal activities. 展开更多
关键词 crystal structure biological activity (R)-3-methyl-2-(4-chlorophenyl)butyric acid 2-amino-6-chloro-4-methoxy-pyrimidine
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Studies on the esterifications of 9-(hydroxyimino)-4-methyl-8,9-dihydrofuro[2,3-h]chromen-2-one with acid chlorides under different conditions
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作者 Ru Shu Sun Yang Wang Peng Xia 《Chinese Chemical Letters》 SCIE CAS CSCD 2008年第7期791-794,共4页
The esterifications of 9-(hydroxyimino)-4-methyl-8,9-dihydrofuro[2,3-h]chromen-2-one (4) with acid chlorides afforded normal oxime-esters 3a-e in 35-78% yields in presence of excessive 4-dimethylaminopyridine as t... The esterifications of 9-(hydroxyimino)-4-methyl-8,9-dihydrofuro[2,3-h]chromen-2-one (4) with acid chlorides afforded normal oxime-esters 3a-e in 35-78% yields in presence of excessive 4-dimethylaminopyridine as the acid scavenger, whereas the reactions gave unexpected 8-substituted products N-(8-chloro-4-methyl-2-oxo-2H-furo-[2,3-h]chromen-9-yl)amides (5a-c) and 4-methyl-2,9-dioxo-8,9-dihydro-2H-furo[2,3-h]chromen-8-ylcarboxyloates (6d-e) by using excessive acid chlorides. The structures of 10 new compounds were determined by 1H NMR, 13C NMR, MS and HRMS, and the possible mechanism for the formation of unexpected products 5a--c and 6d-e was also proposed. 展开更多
关键词 9-(Hydroxyirnino)-4-methyl-8 9-dihydrofuro[2 3-h]chromen-2-one Oxime-ester N-(8-chloro-4-methyl-2-oxo-2H-furo[2 3-h]chro-men-9-yl)amide 4-Methyl-2 9-dioxo-8 9-dihydro-2H-furo[2 3-h]chromen-8-ylcarboxyloate
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A highly enantioselective synthesis of 5- (ι-menthyloxy) -4-substituted-3-chloro-2(5H) -furanones 被引量:1
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作者 耿哲 黄彬 陈庆华 《Chinese Journal of Chemistry》 SCIE CAS CSCD 1999年第2期189-195,共7页
In this paper, stereocontrolled tandem Michael addition-elimination reaction of the novel chiral source, S-(ι-menthyloxy)-3,4-dichloro-2(5H)-furanone, with various thiols and amines has been investigated. A series of... In this paper, stereocontrolled tandem Michael addition-elimination reaction of the novel chiral source, S-(ι-menthyloxy)-3,4-dichloro-2(5H)-furanone, with various thiols and amines has been investigated. A series of new enantiomerically pure compounds, 5-(ι-menthyloxy)-4-substituted-3-cnloro-2(5H)-furanones, were obtained in good yields with d. e.(?)98% under mild conditions. 展开更多
关键词 Tandem Michael addition-elimination reaction 5-(ι-menthyloxy)-3 4-dichloro-2 (5H)-furanone enantiomerically pure compound 5-(ι-menthyloxy)-4-substituted-3-chloro-2(5H)-furanone
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杀虫剂双苯氟脲的合成研究 被引量:5
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作者 周彦峰 高中良 +1 位作者 邱继平 温自强 《河南工业大学学报(自然科学版)》 CAS 北大核心 2008年第1期64-67,共4页
以2-氯-4-硝基苯酚为原料,经还原反应合成2-氯-4-氨基苯酚,再与全氟甲基乙烯基醚加成3-氯-4-[1,1,2-三氟-2-(三氟甲氧基)乙氧基]苯胺;将2,6-二氟苯甲酰胺与草酰氯酰化合成2,6-二氯苯甲酰异氰酸酯,再与3-氯-4-[1,1,2-三氟-2-(三氟甲氧基... 以2-氯-4-硝基苯酚为原料,经还原反应合成2-氯-4-氨基苯酚,再与全氟甲基乙烯基醚加成3-氯-4-[1,1,2-三氟-2-(三氟甲氧基)乙氧基]苯胺;将2,6-二氟苯甲酰胺与草酰氯酰化合成2,6-二氯苯甲酰异氰酸酯,再与3-氯-4-[1,1,2-三氟-2-(三氟甲氧基)乙氧基]苯胺加成得到杀虫剂双苯氟脲,总收率为68.9%. 展开更多
关键词 双苯氟脲 2 6-二氯苯甲酰胺 2-氯-4-硝基苯酚 合成
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催化加氢制备对氯邻氨基苯酚 被引量:5
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作者 单绍军 宋东明 王永灿 《染料工业》 2001年第5期30-31,33,共3页
本文提出了以对氯邻硝基苯酚为原料,使用Raney Ni催化加氢制备对氯邻氨基苯酚,并采用双氰胺为脱氯抑制剂,产品收率达到92.3%。
关键词 催化 加氢 对氯邻氨基苯酚 制备
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高效液相色谱测定单偶氮染料合成中的原料及中间体 被引量:2
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作者 廖艳芳 余慧群 +2 位作者 周海 韦志明 马就庆 《分析科学学报》 CAS CSCD 北大核心 2010年第6期735-737,共3页
采用高效液相色谱法,对以甲酸铬、4-氯-2-氨基苯酚和2-萘酚为原料合成反应产物单偶氮染料进行分析,以体积比为80∶16∶3∶1的乙腈-水-乙酸-三乙胺为流动相,C18柱为固定相,紫外检测器检测波长为313nm。实验探讨了色谱柱、流动相及pH值等... 采用高效液相色谱法,对以甲酸铬、4-氯-2-氨基苯酚和2-萘酚为原料合成反应产物单偶氮染料进行分析,以体积比为80∶16∶3∶1的乙腈-水-乙酸-三乙胺为流动相,C18柱为固定相,紫外检测器检测波长为313nm。实验探讨了色谱柱、流动相及pH值等因素对分离效果的影响,确定了最佳色谱条件。该法对甲酸铬、4-氯-2-氨基苯酚、2-萘酚、反应中间体及单偶氮染料的检出限(S/N=3)分别为0.30、0.12、0.17、0.21、0.05g·L-1,这五种组分回收率为95.9%~102.5%,相对标准偏差(RSD)为0.65%~4.16%。该方法简便快速,准确度高,可用于实际生产质量控制分析。 展开更多
关键词 高效液相色谱法 甲酸铬 4-氯-2-氨基苯酚 单偶氮染料
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Modification on Synthesis of Mixed Ligand Chelates by Using Di- and Trivalent Transition Metal Ions with Schiff Base as Primary Ligand 被引量:1
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作者 Abdussalam Ali Maihub Faten Suliman Alassbaly +1 位作者 Marei Mailoud El-Ajaily Abdunnaser Mohamed Etorki 《Green and Sustainable Chemistry》 2014年第3期103-110,共8页
New mixed ligand chelates synthesized from di-and trivalent metal ions (Cr, Co, Ni, and Cu ions) and Schiff base (L1) resulted from the condensation of 4-dimethylaminobenzaldehyde with 2-aminophenol as primary ligand,... New mixed ligand chelates synthesized from di-and trivalent metal ions (Cr, Co, Ni, and Cu ions) and Schiff base (L1) resulted from the condensation of 4-dimethylaminobenzaldehyde with 2-aminophenol as primary ligand, whereas 2-nitroaniline (L2) represents the secondary ligand in a molar ratio of M:L1:L2 [1:1:1]. The synthesized Schiff base and chelates have been characterized by using several tools, such as, elemental analysis, molar conductivity, magnetic moment measurements, infrared and electronic spectra. The mass spectra of the ligands and Ni(II) chelate were used to justify the process of modification, as well as, the electron paramagnetic resonance spectrum which was carried out for Cu(II) chelate all in order to elucidate the chemical and geometrical structure of the chelates. On the basis of the obtained data, the geometry of the products was proposed for all the chelates. 展开更多
关键词 SCHIFF Base 2-Nitroaniline CHELATES 4-Dimethylaminobenzaaldehyde 2-aminophenol Physiochemical Techniques
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马来酸氟吡汀的合成 被引量:1
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作者 陈宁 《广州化工》 CAS 2016年第13期87-89,共3页
通过对马来酸氟吡汀的合成研究,确定并打通了马来酸氟吡汀的合成路线,该工艺条件与其他路线比较,具有起始原料易得、产品收率高、操作简便等优点。即以2-氨基-3-硝基-6-氯吡啶为原料与对氟苄胺反应,然后氢化还原后,滤液进行酰化反应得... 通过对马来酸氟吡汀的合成研究,确定并打通了马来酸氟吡汀的合成路线,该工艺条件与其他路线比较,具有起始原料易得、产品收率高、操作简便等优点。即以2-氨基-3-硝基-6-氯吡啶为原料与对氟苄胺反应,然后氢化还原后,滤液进行酰化反应得到氟吡汀碱,经五步反应得到马来酸氟吡汀,结构经1H-NMR确认,总收率77%,含量大于99.9%,产品质量符合2010版药典要求。 展开更多
关键词 马来酸氟吡汀 2-amino-6-chloro-3-nitropyridine 4-fluorobenzylamine 合成
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Influence of Meta-Topolin on Efficient Plant Regeneration via Micropropagation and Organogenesis of Safflower (<i>Carthamus tinctorius</i>L.) cv. NARI-H-15
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作者 Jeyachandran Vijayakumar Ponnirul Ponmanickam +2 位作者 P. Samuel D. N. P. Sudarmani J. Pandiarajan 《American Journal of Plant Sciences》 2017年第4期688-705,共18页
The effect of meta-Topolin (mT) was assessed to develop a reliable protocol for efficient plant regeneration of safflower (Carthamus tinctorius L.) cv. NARI-H-15. For micropropagation, 7 - 9 days old shoot-tip explant... The effect of meta-Topolin (mT) was assessed to develop a reliable protocol for efficient plant regeneration of safflower (Carthamus tinctorius L.) cv. NARI-H-15. For micropropagation, 7 - 9 days old shoot-tip explants cultured on MS basal medium supplemented with 3.0 mg/L meta-Topolin (mT) + 0.5 mg/L CPPU showed 97.7% adventitious shoot formation (42.4 shootlets) than node after 45 days of culture. For organogenesis, the seedling explants of immature leaf cultured on 1.5 mg/L CPPU or 1.5 mg/L NAA fortified medium produced high amount of callus than cotyledon and stem calli after 60 days of culture. However, MS basal medium fortified with 4.0 mg/L mT + 1.5 mg/L CPPU was found beneficial to stimulate 100% organogenic response (74.7 shootlets) from immature leaf calli than cotyledon and stem derived calli after 45 days of culture. The healthy plantlets obtained from micropropagation and organogenesis process cultured on 1/4 MS basal salts, 1.5% sucrose (w/v) and 0.8% agar (w/v) medium supplemented with NAA (1.5 mg/L) and mT (0.1 mg/L) produced maximum of 96% (12.8 rootlets) and 84% (7.3 rootlets) adventitious rooting, respectively than mT and CPPU tested medium. However, maximum of 67% and 42% survival rate was noticed when in vitro raised plants from micropropagation and organogenesis were hardened in pots containing soil mix and maintained under green house condition. This optimized regeneration protocol might be helpful in regeneration of new genotypes and cultivars of safflower to improve agronomic traits through in vitro selection process and Agrobacterium-mediated genetic transformation system. 展开更多
关键词 CARTHAMUS Tinctorius L. Meta-Topolin N-(2-chloro-4-pyridyl-N’-phenylurea) MICROPROPAGATION ORGANOGENESIS
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2-酯基-1,5-苯并氧氮杂的合成及反应副产物的研究 被引量:1
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作者 刘倩 赵利飞 +1 位作者 李文红 李媛 《有机化学》 SCIE CAS CSCD 北大核心 2012年第11期2122-2128,共7页
以取代苯、丁烯二酸酐、邻氨基(对氯邻氨基)苯酚为原料,合成了一系列2-酯基-1,5-苯并氧氮杂衍生物,其结构通过IR,1H NMR,MS(HRMS)及元素分析进行表征.同时,确定了一个主要副产物2-苯甲酰甲基-2H-1,4-苯并噁嗪-3(4H)-酮(6h')的结构,... 以取代苯、丁烯二酸酐、邻氨基(对氯邻氨基)苯酚为原料,合成了一系列2-酯基-1,5-苯并氧氮杂衍生物,其结构通过IR,1H NMR,MS(HRMS)及元素分析进行表征.同时,确定了一个主要副产物2-苯甲酰甲基-2H-1,4-苯并噁嗪-3(4H)-酮(6h')的结构,提出了其可能的生成机理.研究还表明,中间体4-芳基-4-氧代-2-丁烯酸酯(4)在对甲基苯磺酸为催化剂、DMF作溶剂、回流温度下反应时主要生成目标产物2-酯基-1,5-苯并氧氮杂6,而在冰醋酸为催化剂、甲醇作溶剂、回流温度下反应时则主要生成副产物6h'. 展开更多
关键词 迈克尔加成 1 5-苯并氧氮杂 2-氨基苯酚 4-氯-2-氨基苯酚 反应机理
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