CAS: 20260-53-1; Nicotinoyl Chloride Hydrochloride

该化合物是一种化学化合物,其特点是其丙烯环结构,这是一个由六人组成的芳香环,含有一个氮原子.该化合物的特点是碳基氯化物功能组,表明存在碳原子,该原子的双壳与氧原子和氯原子的单壳同时存在.盐酸形式表明,该化合物是盐酸形成的盐,提高了其在水中的溶解性.一般而言,该物质是白色至非白色固体,因其再活动作用而闻名,特别是由于碳基氯化物组的电极性,在核生殖替代反应中尤为如此.它经常用于有机合成,特别是在制作各种丙烯衍生物和其他外环环化合物时.在处理该化合物时,安全防范是不可或缺的,因为它可以是腐蚀性的,并且可能在分解时释放出有毒气体.建议从湿和不相容物质进入一个冷,干的地方进行适当储存,以便保持其稳定性.

结构式图片

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39620-02-5 58757-38-3 49609-84-9

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合成工艺路线路线简述

    烟酸置于氯化亚砜体系中,化学反应 4.0H,以100%的收率获得氯化烟碱盐酸盐
    参考文献:Homochiral Crystallization Of Helical Coordination Chains Bridged By Achiral Ligands: Can It Be Controlled By The Ligand Structure
    标题:Homochiral Crystallization Of Helical Coordination Chains Bridged By Achiral Ligands: Can It Be Controlled By The Ligand Structure
    摘要:描述了通过非手性的多吡啶配体连接的螺旋手性聚合物链的同手性/异手性结晶过程,这一过程取决于连接配体的结构,而与溶剂无关,暗示了一种设计螺旋链非手性晶体的潜在策略,即使用手性连接配体.
    Doi:10.1039/b416412A

    海关参考信息

    专利信息


    专利号:US-6423847-B1
    优先权日:1999-04-07
    标题:Synthesis and clinical uses of D,α-tocopherol nicotinate compounds
    发明人:PEARSON DON C; RICHARDSON KENNETH T
    权利人:CHRONORX LLC
    摘要:A process of synthesis of D,alpha-tocopherol nicotinate compounds is presented. Therapeutic uses for this compound are described. The active agents are demonstrated to be complementary in their physiological functions especially as these relate to cellular and endothelial biochemistry and physiology and, ultimately to vascular health. The active components of the invention are selected for inclusion in a unique combination that clinically reduces risks of vasculopathy, DNA strand breakage and neuronal excitotoxicity in various diseases. In addition to the systemic vascular benefits acquired, improvement of the vascular health of the eye reduces the risk of glaucomatous optic nerve atrophy with its accompanying visual field loss and potential blindness and reduces conditions of risk for macular degeneration.

    专利号:US-6693122-B2
    优先权日:1999-05-12
    标题:Nitrosated and nitrosylated potassium channel activators, compositions and methods of use
    发明人:GARVEY DAVID S; SAENZ DE TEJADA INIGO
    权利人:NITROMED INC
    摘要:The present invention describes novel nitrosated and/or nitrosylated potassium channel activators, and novel compositions comprising at least one nitrosated and/or nitrosylated potassium channel activator, and, optionally, at least one compound that donates, transfers or releases nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor, stimulates endogenous synthesis of nitric oxide or is a substrate for nitric oxide synthase and/or at least one vasoactive agent. The present invention also provides novel compositions comprising at least one potassium channel activator, and at least one compound that donates, transfers or releases nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor, stimulates endogenous synthesis of nitric oxide or is a substrate for nitric oxide synthase and/or at least one vasoactive agent. The present invention also provides methods for treating or preventing sexual dysfunctions in males and females, for enhancing sexual responses in males and females, and for treating or preventing cardiovascular disorders, cerebrovascular disorders, hypertension, asthma, baldness, urinary incontinence, epilepsy, sleep disorders, gastrointestinal disorders, migraines, irritable bowel syndrome and sensitive skin.

    专利号:US-2013035307-A1
    优先权日:2010-01-26
    标 题:Methods for treating or preventing the spread of cancer using semi-synthetic glycosaminoglycosan ethers
    发明人:PRESTWICH GLENN D; KENNEDY THOMAS P
    权利人:UNIV UTAH RES FOUND; PRESTWICH GLENN D; KENNEDY THOMAS P
    摘要:Described herein are methods for the treatment and prevention of tumor metastasis using alkylated and fluoroalkylated semi-synthetic glycosaminoglycan ethers (“SAGEsâ€?). The synthesis of sulfated alkylated and fluoroalkylated SAGEs is also described.

    专利号:US-9453037-B2
    优先权日:2011-07-28
    标 题 :Methylphenidate-prodrugs, processes of making and using the same
    发明人:GUENTHER SVEN; CHI GUOCHEN; BERA BINDU; MICKLE TRAVIS; BERA SANJIB
    权利人:KEMPHARM INC; KEMPHARM INC
    摘要:The present technology is directed to prodrugs and compositions for the treatment of various diseases and/or disorders comprising methylphenidate, or methylphenidate derivatives, conjugated to at least one alcohol, amine, oxoacid, thiol, or derivatives thereof. In some embodiments, the conjugates further include at least one linker. The present technology also relates to the synthesis of methylphenidate, or methylphenidate derivatives, conjugated to at least one alcohol, amine, oxoacid, thiol, or derivatives thereof or combinations thereof.

    专利号:US-4021436-A
    优先权日:1974-03-15
    标题 :Derivatives of nicotinic acid with amines variously substituted
    发明人:CAVAZZA CLAUDIO
    权利人:CAVAZZA CLAUDIO
    摘要:A novel thionicotinate of nicotinamide is disclosed having the formula: ##STR1## The compound has the useful pharmacological activity of lowering cholesterol, free fatty acid and triglyceride plasma levels. In cases of liver injury, administration of the compound has modified toward normal the injury-induced malfunction of the liver. A synthesis of the compound from nicotinoyl chloride hydrochloride is described as well as modes for the administration of the compound.

    专利号:US-4021433-A
    优先权日:1973-03-08
    标 题:Derivative of nicotinic acid with amides
    发明人:CAVAZZA CLAUDIO
    权利人:SIGMA TAU IND FARMACEUTI
    摘要:A novel cysteine thiolactone of nicotinamide is disclosed having the formula: ##STR1## The compounds, homo-cysteine thiolactone of nicotinamide, and its pharmacologically acceptable salts have the useful pharmacological activity of lowering cholesterol, free fatty acid and triglyceride plasma level in the case of altered lipid metabolism and improving BSP clearance ratio in cases of liver injury. n A synthesis of the compound from nicotinoyl chloride, hydrochloride or nicotinic acid esters is described as well as modes for the administration of the compound.
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    合成参考文献


    摘要:Kleemann, A.; Engel, J.; Kutscher, B.; Reichert, D., Pharmaceutical Substances[Online], Thieme: Stuttgart, (2003).
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