CAS: 74936-71-3; 1,4-Dihydro-2,6-Dimethyl-4-(2'-Nitrophenyl)-Pyridine-3,5-Dicarboxylic Acid Monomethyl Ester

该化合物是一种二丙烯衍生物,在制药和化学研究中具有显著应用,其结构具有硝基苯组和酯功能,使其成为合成钙管阻塞器和其他生物活性化合物的宝贵中间体.复合物在受控条件下表现出稳定性,并显示出由于其反应场所而进一步发挥作用的潜力.其定义明确的分子结构允许精确的修改,支持其在药物开发和机械研究中的使用.硝基体组的存在增强了其在减少硝基反应中的效用,扩大了其在合成化学中的应用性.

结构式图片

MSDS等安全信息

    上下游产品

    1,4-Dihydro-2,6-Dimethyl-3-Methoxycarbonyl-4-(2-Nitrophenyl)-5-(2-Cyanoethoxy)-Carbonyl-Pyridine 75150-43-5

    合成工艺路线路线简述

    • 21829-25-4 = 74936-71-3
      反应条件:1.1R:Nah,S:Dmf2.1R:Koh,S:Meoh3.1R:HCL,S:H2O,S:Me2Co
      标题:Radiosynthesis Of [11C]Nifedipine And [11C]Nicardipine
      作者:By Wilson,Alan A. Et Al
      参考文献:Journal Of Labelled Compounds And Radiopharmaceuticals 日期:1989 卷标:27(5) 页码:589-98]

      39562-27-1 + 43107-08-0 = 74936-71-3
      反应条件:1.1S:Etoh,Reflux2.1R:Naoh,S:H2O,S:Me2Co,Cooled; 2 H,Rt
      标题:Synthesis And Characterization Of 4-Aryl-1,4-Dihydropyridine-3,5-Dicarboxylates
      作者:By Wu,Xiao-Yun Et Al
      参考文献:Youji Huaxue 日期:2006 卷标:26(1) 页码:93-98]

      312494-91-0 = 74936-71-3
      反应条件:1.1S:Thf1.2R:Et3N,R:Me3Siso3Cf3
      标题:Strategies For The Synthesis Of Nifedipine Analogous Esters From L-Ascorbic Acid
      作者:By Gorlitzer,K. And Baltrusch,H. J.
      参考文献:Pharmazie 日期:2001 卷标:56(3) 页码:208-213]

      75150-43-5 = 74936-71-3
      反应条件:1.1
      标题:Biotransformation Of Nifedipine In Rat And Dog
      作者:By Scherling,D. Et Al
      参考文献:Arzneimittel-Forschung 日期:1992 卷标:42(11) 页码:1292-300
    📜β-氨基巴豆酸甲酯置于lithium Hydroxide Monohydrate体系中,用 乙醇 作为反应溶剂,化学反应 2.0H,反应生成 硝苯地平杂质h
    参考文献:化合物及其作为l-型钙通道阻滞剂或/和乙酰 胆碱酯酶抑制剂的应用
    标题:化合物及其作为l-型钙通道阻滞剂或/和乙酰 胆碱酯酶抑制剂的应用
    摘要:本发明公开了化合物及其作为l-型钙通道阻滞剂或/和乙酰胆碱酯酶抑制剂的应用.100Nmol/l的本发明所述化合物对l-型钙通道的抑制率为8.71-35.77%,1000Nmol/l的本发明所述化合物对l-型钙通道的抑制率为26.43-83.54%,本发明所述化合物对乙酰胆碱酯酶活性的ic50为16-1470Nmol/l,可见,本发明所述化合物对l-型钙通道具有有效地阻滞作用,对乙酰胆碱酯酶具有明显的抑制作用,因此,本发明还提供所述化合物在制备治疗心血管疾病,中风或老年性痴呆药物中的应用.

    海关参考信息

    专利信息


    专利号:WO-9319076-A1
    优先权日:1992-03-20
    标题:θ6 METAL COMPLEXES OF 4-ARYL-1,4-DIHYDROPYRIDINES
    发明人:NATALE NICHOLAS R; BITTERWOLF THOMAS E; HUBLER TIMOTHY
    权利人:IDAHO RES FOUND
    摘要:The present invention is directed to θ6 metal complexes of the arene group of 4-aryl-1,4-dihydropyridines. The 4-aryl-1,4-dihydropyridines are made according to the Hantzsch pyridine synthesis, and are then reacted with a Ï€ acid ligand-metal reagent to attach the metal in an θ6 fashion to the 6Ï€ electrons of the arene ring. The 4-aryl-1,4-dihydropyridine metal complexes are designed to provide useful spectroscopic information concerning the conformation of the 4-aryl-1,4-dihydropyridines and how such compounds interact with the calcium channel protein. Moreover, the 4-aryl-1,4-dihydropyridine metal complexes are robust calcium antagonists and compare to or exceed the biological activity of previously known calcium channel antagonists.

    专利号:EP-1532110-B1
    优先权日:2002-07-01
    标题 :Industrial process for the synthesis of isobutyl methyl 1,4-dihydro-2,6-dimethyl-4-(2-nitrophenyl)-3,5-pyridine dicarboxylate (nisoldipine)

    专利号:EP-1532110-A1
    优先权日:2002-07-01
    标 题:Industrial process for the synthesis of isobutyl methyl 1,4-dihydro-2,6-dimethyl-4-(2-nitrophenyl)-3,5-pyridine dicarboxylate (nisoldipine)

    专利号:WO-2004002958-A1
    优先权日:2002-07-01
    标题 :Industrial process for the synthesis of isobutyl methyl 1,4-dihydro-2,6-dimethyl-4-(2-nitrophenyl)-3,5-pyridine dicarboxylate (nisoldipine)

    专利号:US-5258519-A
    优先权日:1990-11-13
    标 题:Dihydropyridine vasodilators agents
    发明人:WHEELER THOMAS N; KENAKIN TERRENCE P
    权利人:GLAXO INC
    摘要:Compounds of the following formula (I): (I) where R1 and R2 are alkyl or cycloalkyl, which may be substituted, R4 is aryl such as phenyl which may be substituted, L is a direct bond or an oxygen containing linking group, R is a hydrogen, alkyloxy, alkyl, halogen or haloalkyl and Het is a pyridinyl or pyridazinyl group. The compounds can be used antihypertensives or myocardial relaxants. Also part of the invention are pharmaceutical compositions, intermediates and methods of synthesis.

    专利号:US-5100892-A
    优先权日:1990-11-13
    标 题 :Dihydropyridine vasodilator agents
    发明人:WHEELER THOMAS N; KENAKIN TERRENCE P
    权利人:GLAXO INC
    摘要:Compounds of the following formula (I): (I) where R1 and R2 are alkyl or cycloalkyl, which may be substituted, R4 is aryl such as phenyl which may be substituted, L is a direct bond or an oxygen containing linking group, R is a hydrogen, alkyloxy, alkyl, halogen or haloalkyl and Het is a pyridinyl or pyridazinyl group. The compounds can be used antihypertensives or myocardial relaxants. Also part of the invention are pharmaceutical compositions, intermediates and methods of synthesis.

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    品牌试剂参考报价(招募中)

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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:S113 | SWISSPHARMA24 | 2024 Swiss Pharmaceutical List with Metabolites | DOI:10.5281/zenodo.10501043
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