CAS: 20041-90-1; N,1-Dimethyl-4-(Methylamino)-1H-Imidazole-5-Carboxamide

该化合物是属于一分子衍生物类别的化学化合物,该物质具有五人组成芳香环,含有两个氮原子,有助于其基本性和潜在的生物活动;二甲基和甲基氨基组的存在增强了其亲脂性,有可能影响其溶性及生物系统中的渗透性;碳箱胺功能组表明,它可以参与氢联结,这可能影响其与生物目标的相互作用;该化合物可能具有药理特性,使其对医药化学和药物开发具有兴趣;其结构特征表明,它有可能在各个领域,包括制药领域,作为进一步调整其功效和选择性的导料化合物;许多化学物质,了解其特性,反应性和生物相互作用对于其在研究和工业中的应用至关重要.

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3,7-dihydro-1,3,7-trimethyl-1H-purine-2,6-dione formaldehyd methylamine-1-methyl-5-methylamin°Carbonylimidazole4--1-methyl-5-methylamin°Carbonylimidazole imidazole1-methyl-5-methylamin°Carbonyl-4-imidazole -N-methylamino>imidazole1-methyl-5-methylamin°Carbonyl-4--N-methylaminoimidazole 1,3,7-Trimethyl-2-(3-nitro-phenyl)-1,2,3,7-tetrahydro-purin-6-one

合成工艺路线路线简述

    📜Alkaline Earth Salt Of/the/ Methylsulfuric Acid置于水体系中,化学反应生成咖啡啶
    参考文献:Einhorn; Baumeister,Chemische Berichte,1898,Vol. 31,P. 1138
    标题:Einhorn; Baumeister,Chemische Berichte,1898,Vol. 31,P. 1138

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    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:Synthesis Of Imidazo(4,5-E)(1,4)Diazepine And Imidazo(4,5-E)(1,4)Oxazepine Derivatives Using Caffeidine, A Hydrolysis Product Of Caffeine.
    作者:Tsutomu Ohsaki,Takeo Kuriki,Taisei Ueda,Jinsaku Sakakibara,Masahisa Asano
    摘要:Synthesis Of Imidazo[4, 5-E][1, 4]Diazepines Using Caffeidine (1) Was Studied. Caffeidine Was Condensed With Various α, β-Unsaturated Carboxylic Acid Derivatives To Give N-(α, β-Unsaturated Acyl)Caffeidines (4). Intramolecular Michael Addition Of 4 Having An Electron-Withdrawing Group At The β-Position Of The α, β-Unsaturated Acyl Group Afforded Imidazo[4, 5-E][1, 4]Diazepines (5, 6). Compounds Of The Same Type (14) Were Also Prepared By Treatment Of N-(α-Halogenoacyl)Caffeidines (13) With Etona In Abs. Etoh. On The Other Hand, Heating Of 13 In H2O Gave Imidazo[4, 5-E][1, 4]Oxazepines (15). Compounds 5D, 15B, And 15C Showed Arterial Relaxing Activities.

    合成参考文献


    摘要:R.M. Hoskinson. Australian J. Chem. 21, 1913 (1968).
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