共查询到20条相似文献,搜索用时 15 毫秒
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由3-羟基丙腈与叠氮化铵采用超声波辐射技术经1,3-偶极环化加成获得母体化合物5-羟乙基四唑;母体化合物与硫酸二甲酯经取代反应得到中间体甲基-5-羟乙基四唑,然后甲基-5-羟乙基四唑再与氯化亚砜经卤代反应得到中间体2-甲基-5-氯乙基四唑,收率为68%;2-甲基-5-氯乙基四唑在碱性条件下经消除反应生成2-甲基-5-乙烯基四唑,收率为75%。采用红外光谱、核磁共振、元素分析等对2-甲基-5-氯乙基四唑、2-甲基-5-乙烯基四唑进行了结构表征。该法具有反应收率较高且稳定、易操作等优点。 相似文献
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The pure mononitro derivative of benzimidazolone-2 can be obtained only when the nitration reaction is carried out in mild conditions, otherwise di-, tri- and tetranitro derivatives are also formed. The results of our studies derived optimum conditions for the nitration process necessary to obtain pure 5-nitrobenzimidazolone-2. 相似文献
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利用3-甲基吡啶为原料,通过光氯化反应合成并分离出了2-氯-5-三氯甲基吡啶。探讨了光氯化反应的机理,通过正交实验对其工艺进行优化,得到了合成产物的最佳工艺条件:温度为180℃,时间为10h,原料与溶剂体积比为1:3,产物产率可达到53.1%。同时用IR、^1HNMR、^13CNMR、MS、UV—Vis等光谱手段确定了产品的结构。 相似文献
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Dr. Swagat Sharma Dr. Juan L. Pablo Kirsten T. Tolentino Wacey Gallegos Jennifer Hinman Madison Beninato MacKenzie Asche Dr. Anna Greka Dr. Corey R. Hopkins 《ChemMedChem》2022,17(14):e202200151
The transient receptor potential cation channel 5 (TRPC5) plays an important role in numerous cellular processes. Due to this, it has gained considerable attention over the past few years as a potential therapeutic target. Recently, TRPC5 has been shown to be involved in the regulation of podocyte survival, indicating a potential treatment option for chronic kidney disease. In addition, a recent study has shown TRPC5 to be expressed in human sensory neurons and suggests that TRPC5 inhibition could be an effective treatment for spontaneous and tactile pain. To understand these processes more fully, potent and selective tool compounds are needed. Herein we report further exploration of the 2-aminobenzimidazole scaffold as a potent TRPC5 inhibitor, culminating in the discovery of 16 f as a potent and selective TRPC5 inhibitor. 相似文献
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以对硝基甲苯为起始原料,经磺化、氧化、重氮化等步骤合成了10个新型5-取代苯磺酰胺类化合物。经1HNMR、MS及元素分析确证了目标化合物的结构。 相似文献
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氯虫苯甲酰胺的合成及表征 总被引:1,自引:0,他引:1
以3-甲基-2-硝基苯甲酸为原料通过RaneyNi加氢还原制得3-甲基-2-氨基苯甲酸,接着与N-氯代丁二酰亚胺(NCS)反应制得3-甲基-2-氨基-5-氯苯甲酸,然后3-甲基-2-氨基-5-氯苯甲酸与氯化亚砜在75~80℃下回流3h后,接着缓慢滴加甲胺水溶液,在室温下搅拌反应12h,得到2-氨基-5-氯-N,3-二甲基甲酰胺。然后再与3-溴-1-(3-氯吡啶-2-吡啶基)-1 H-吡唑-5-甲酸在-5~0℃下滴加甲基磺酰氯反应得到产品氯虫苯甲酰胺,四步总收率37.0%,产品HPLC纯度是96.05%。 相似文献
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发展了一例2-炔基苯甲醛肟与5-氯苯并咪唑在三氟甲磺酸银催化下的串联反应。反应在加入三吡咯烷基溴化鏻六氟磷酸盐活化氮氧叶立德之后,5-氯苯并咪唑作为亲核试剂进攻异喹啉中间体B的1-位,最后芳构化得最终产物。该反应对底物官能团的兼容性良好,能在温和的条件下以中等的收率合成两种未曾报道的1-苯并咪唑基异喹啉化合物。所得目标产物均经1 HNMR、13 CNMR、 HRMS确认。 相似文献
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以三乙醇胺为模板剂, 采用静态晶化水热法合成出一种特殊结构的沸石分子筛 (称作SAO-25) , 合成过程中不易发生混晶和转晶, 重复性良好。对SAO-25 沸石进行了物相分析和红外光谱研究, 考察了它的吸附性能和酸性。在SAO-25 沸石分子筛上进行正构烷烃 (n2-C6) 裂解反应测试, 显示出较高的催化活性; 在重油裂解反应测试中, 显示出很高的C=3、C=4 轻烯烃选择性。 相似文献
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Laura Amores-Bonet Ralf Kleene Thomas Theis Melitta Schachner 《International journal of molecular sciences》2022,23(17)
The neural cell adhesion molecule (NCAM) plays important functional roles in the developing and mature nervous systems. Here, we show that the transient receptor potential canonical (TRPC) ion channels TRPC1, −4, and −5 not only interact with the intracellular domains of the transmembrane isoforms NCAM140 and NCAM180, but also with the glycan polysialic acid (PSA) covalently attached to the NCAM protein backbone. NCAM antibody treatment leads to the opening of TRPC1, −4, and −5 hetero- or homomers at the plasma membrane and to the influx of Ca2+ into cultured cortical neurons and CHO cells expressing NCAM, PSA, and TRPC1 and −4 or TRPC1 and −5. NCAM-stimulated Ca2+ entry was blocked by the TRPC inhibitor Pico145 or the bacterial PSA homolog colominic acid. NCAM-stimulated Ca2+ influx was detectable neither in NCAM-deficient cortical neurons nor in TRPC1/4- or TRPC1/5-expressing CHO cells that express NCAM, but not PSA. NCAM-induced neurite outgrowth was reduced by TRPC inhibitors and a function-blocking TRPC1 antibody. A characteristic signaling feature was that extracellular signal-regulated kinase 1/2 phosphorylation was also reduced by TRPC inhibitors. Our findings indicate that the interaction of NCAM with TRPC1, −4, and −5 contributes to the NCAM-stimulated and PSA-dependent Ca2+ entry into neurons thereby influencing essential neural functions. 相似文献
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以2-溴-1-(2-噻吩)-1-乙酮和对-甲基苯甲胺为原料,在复合催化剂碘与叔丁基过氧化氢的作用下,通过氧化环合反应合成了5-(2-噻吩)-2-对-甲苯基噁唑。产物结构经FTIR,NMR 和MS检测。结果显示:合成产物的最佳条件为:2-溴-1-(2-噻吩)-1-乙酮1 mmol、对-甲基苯甲胺1.3 mmol、碘0.2 mmol、质量分数55%的叔丁基过氧化氢1.2mmol、碳酸氢钠1.0 mmol,室温下反应12 h,产物收率为89.7 %。抑菌圈测定结果显示该产物对大肠杆菌具有强的抑菌能力。 相似文献