CAS: 10261-94-6; 3-Nitro-2-Pyridinecarboxaldehyde

该化合物是一种有机化合物,其特征是其丙烯酯环,这是一个六人组成的芳香热循环,含有一个氮原子; 硝基甲基苯基(-NO2)存在于3位置,而甲酰胺(-CHO)在2位置,有助于其反应和功能特性; 这种化合物一般是黄到褐的固体或液体,取决于其纯度和形态; 极地有机溶剂溶解于极地有机溶剂,使其在各种化学反应中有用,特别是在合成更复杂的有机分子方面. 硝基甲基苯可参与生物替代反应,而甲酰胺组则可以进行核分裂性添加反应. 3-硝基苯基丁-2-碳酸丁,由于潜在的生物活动,经常用于制药工业和农用化学的开发.在处理这一化合物时,应当注意安全防范措施,因为它可能对健康造成危害,包括对皮肤和呼吸系统产生刺激.

结构式图片

相似化合物

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合成工艺路线路线简述

    📜2-甲基吡啶氧化物置于磷酸,Potassium Carbonate,4-硝基苯甲酰氯,Silver Nitrate,二甲基亚砜,N,N'-二环己基碳二亚胺体系中,用 甲醇 用作溶剂,化学反应 4.0H,反应生成3-硝基吡啶-2-甲醛
    参考文献:新型1,4-二氢吡啶类钙拮抗剂.I.4-(取代的吡啶基)-1,4-二氢吡啶衍生物的合成和降血压活性.
    标题:新型1,4-二氢吡啶类钙拮抗剂.I.4-(取代的吡啶基)-1,4-二氢吡啶衍生物的合成和降血压活性.
    摘要:合成了一系列4-(取代的吡啶基)-1,4-二氢吡啶衍生物,并研究了它们的降压作用.几种化合物,2-(n-苄基-N-甲基氨基)乙基甲基1,4-二氢-2,6-二甲基-4-(3-硝基-2-吡啶基)-3,5-吡啶二甲酸(2B),4-(4-硝基-2-吡啶基)类似物(2G),4-(3-三氟甲基-2-吡啶基)类似物(2C),4-(2-三氟甲基-3-吡啶基)类似物(3E),4-发现(4-氰基-2-吡啶基)类似物(2E),4-(2-氰基-3-吡啶基)类似物(3D)和4-(6-溴-2-吡啶基)类似物(2I)具有与尼卡地平类似的降压活动;特别是2C和3E的持续时间约为尼卡地平的两倍,而2E具有在所有合成衍生物中最有效的降压活性.
    Doi:10.1248/cpb.38.2446

    专利信息


    专利号:WO-2008022467-A1
    优先权日:2006-08-25
    标 题 :2-substituted azain doles and 2 substituted thienopyrroles, their precursors and novel processes for the preparation thereof
    发明人:LAUTENS MARK; YUEN JOSEPHINE; FANG YUANQING
    权利人:LAUTENS MARK; YUEN JOSEPHINE; FANG YUANQING
    摘要:The present invention relates generally to processes for the chemical synthesis of azaindole and thienopyrrole compounds, in particular azaindole and thienopyrrole compounds that are substituted at the 2-position of the azaindole or thienopyrrole ring, and optionally at additional locations of the azaindole or thienopyrrole ring such as the 1- and/or 3-position, compounds prepared by such processes, and synthetic precursors of such processes. More particularly, the present invention relates to the preparation of 2- substituted azaindoles from an ortho-gem-dihalovinylaminopyridine or from an ortho- gem-dihalovinylaminopyridine N-oxide compound and an organoboron reagent using a palladium metal pre-catalyst, base and a ligand. The present invention also relates to the preparation of 2-substituted thienopyrroles from an ortho-gem-dihalovinylthiophene compound and an organoboron reagent using a palladium metal pre-catalyst, base and a ligand. The present invention also relates to processes for the production of ortho-gem- dihalovinylaminopyridines which are useful as starting materials in the production of 2- substituted azaindoles, and novel compounds prepared by the processes. The present invention also relates to processes for the production of ortho-gem-dihalovinylthiophenes which are useful as starting materials in the production of 2-substituted thienopyrroles, and novel compounds prepared by the processes. Formulae (V) and (VII).

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:Synthesis Of 3-Aminopyridine-2-Carboxaldehyde Thiosemicarbazone (3-Ap)
    作者:Chuansheng Niu,Jun Li,Terrence W. Doyle,Shu-Hui Chen |发布日期:1998.6
    摘要:Methylboronic Acid With 2-Chloro-3-Nitropyridine Produced 2-Methyl-3-Nitropyridine 4 In One Step In High Yield. Oxidation Of 4 With Selenium Dioxide Gave Aldehyde 5. Alternatively, Condensation Of 4 With Dmfdma Followed By Oxidation Gave 5 In A Two Step Higher Yielding Conversion. Subsequent Direct Coupling Of 5 With Thiosemicarbazide Followed By Reduction Of The Nitro Group Using Stannous Chloride Or Sodium

    合成参考文献


    摘要:Andersson, C.-M.; Andersson, M., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 3, 42.
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