CAS: 2196-13-6; Pyridine-4-Carbothioamide

该化合物是一种属于硫酰胺类的化学化合物,其特点是存在硫酰胺功能组,由硫磺原子结为碳原子,与氮原子相连.该化合物在结构上与氮原子有关,主要与氨基氧组取代硫磺原子不同.Thioisonicotinimide展示了硫酰胺的典型特性,包括在各种化学反应中的潜在再活动,例如核循环替代和与金属离子的协调.该化合物还可能显示生物活动,使其对药物研究感兴趣.该化合物一般为在室温度下固态,并可能具有取决于所用溶剂的具体溶解性特征.与许多硫化物一样,处理硫酰胺十分重要,因为潜在的毒性和再活性而需要小心处理硫酰胺.其应用可能延伸到药物开发的化合物.

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CAS号1453-82-3 异烟碱 | CAS号100-48-1 4-氰基吡啶 | CAS号696-54-8 4-吡啶甲醛肟 | CAS号108103-05-5 dithioisonicoti... | CAS号872-85-5 4-吡啶甲醛 | CAS号106950-18-9 4-Phenyl-2-(4-p... | CAS号3731-53-1 4-甲氨基吡啶 | CAS号1822-53-3 4-吡啶甲硫醇 | CAS号21346-36-1 2-(吡啶-4-基)-1,3-... | CAS号21278-85-3 2-(吡啶-4-基)噻唑-4-羧酸乙酯 | CAS号100-48-1 4-氰基吡啶 | CAS号581-47-5 2,4'-联吡啶 | CAS号15311-09-8 2,5-双(4-吡啶基)-1,... | CAS号89830-71-7 4-吡啶甲亚胺酸肼 | CAS号1453-82-3 异烟碱

合成工艺路线路线简述

    4-吡啶甲酰胺置于水体系中,用 水 用作溶剂,化学反应生成硫代异烟酰胺
    参考文献:在水性介质中无金属,一锅法将醛氧化转化为伯硫代酰胺
    标题:在水性介质中无金属,一锅法将醛氧化转化为伯硫代酰胺
    摘要:摘要 多种醛与氨水,分子碘和 O,O-二乙基二硫代磷酸的一锅串联反应容易得到相应的伯硫代酰胺.这是一种廉价,实用且无金属的方法,可以在水性介质中从醛中获取各种硫代酰胺.简单地通过过滤然后用硫代硫酸钠水溶液和水连续洗涤来获得纯产物.[本文提供补充材料.访问出版商的 Synthetic Communications® 在线版,获取以下免费补充资源:完整的实验和光谱细节.] 图形摘要
    Doi:10.1080/00397911.2013.808350

    海关参考信息

    专利信息


    专利号:EP-4423083-A2
    优先权日:2021-11-29
    标 题:Synthesis of pyrazolone derivative compounds and their effects on cox enzymes
    发明人:ÖNAY UÇAR EVREN; DEM RAYAK EREF; BERK BARKIN; YURTTA LEYLA; B LTEK N KALEL SEVDE NUR; AH N ZAFER
    权利人:UNIV ISTANBUL MEDIPOL; ISTANBUL UNIV REKTORLUGU; ANADOLU UNIV
    摘要:The invention is related to the synthesis of 8 pyrazolone derivative compounds and their activities on COX enzymes.

    专利号:CN-107250144-A
    优先权日:2014-12-19
    标题:Total synthesis of triancorubin DC-45-A2 and preparation of triancorubin analogs

    专利号:WO-2023096623-A2
    优先权日:2021-11-29
    标题:Synthesis of pyrazolone derivative compounds and their effects on cox enzymes

    专利号:CN-108374182-B
    优先权日:2018-02-27
    标题 :A New Method for Electrochemical Synthesis of 1,2,4-Thiadiazole Compounds

    专利号:CN-108374182-A
    优先权日:2018-02-27
    标题 :A New Method for Electrochemical Synthesis of 1,2,4-Thiadiazole Compounds
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    主要参考文献

    参考标题:Synthesis And Characterizations Of Novel Thiazolyl-Thiadiazole Derivatives As Telomerase Activators
    作者:Kayagil, Ismail,Mutlu, Ayşe Gül,Bayhan, ülkü,Yilmaz, Inanç,Demirayak, şeref
    摘要:Pyridine-3/4-Thiocarboxamide Derivatives Were Used As Starting Materials For The Synthesis Of The Target Compounds. The Pyridine-3/4-Thiocarboxamide Derivatives Were Reacted With Ethyl 2-Chloroacetoacetate In Ethanol To Give The Thiazole Derivatives (1, 2). The Two Ethyl Thiazole-Carboxylate Derivatives (1, 2) Thus Obtained Were Treated With Sodium Hydroxide Solution And Ethanol And Converted To Carboxylic Acids (3, 4). The Carboxylic Acid Derivatives (3, 4) Were Reacted With Thiosemicarbazide In Phosphoroxy Trichloride And Aminothiadiazole Rings (5, 6) Were Formed. Thus, Two Thiazolyl-Thiadiazole Amine Derivatives (5, 6) Were Obtained. These Two Derivatives (5, 6) Were Converted Into Two Chloroacetamidothiadiazole Derivatives (7, 8) By Reaction With Chloroacetylchloride Over The Amino Group In The Presence Of Triethylamine In Acetone. After All These Steps, The Starting Materials (7, 8) Needed To Reach The Target Compounds Were Obtained. With The Two Derivatives (7, 8) Obtained In This Last Step, Phenol And Thiophenol Derivatives Were Reacted In Acetone In The Presence Of Potassium Carbonate. The Target Compounds, Thiazolyl-Thiadiazole Derivatives (Tda$_\mathbf1-16}})$, Are Completely Unique And Their Structure Has Been Elucidated By Elemental Analysis, Ir, Nmr, And Ms Spectral Data. After All These Synthesis Steps, Telomerase Activity Studies Were Performed On The Target Compounds Obtained. For This Purpose, A Pcr Elisa-Based Trap Method Was Used On The Heart Of Zebrafish. According To The Enzyme Assay Results, Derivative Tda$_\mathbf8}}$ Has Shown An Increase Of Telomerase Enzyme Activity.

    合成参考文献


    摘要:National Technical Information Service., AD691-490
    摘要:Journal of Organic Chemistry., 19(753), 1954
    摘要:Tang, R.-Y., Science of Synthesis: Knowledge Updates, (2024) 1, 412.
    摘要:Tang, R.-Y., Science of Synthesis: Knowledge Updates, (2024) 1, 357.
    摘要:Tang, R.-Y., Science of Synthesis: Knowledge Updates, (2024) 1, 377.
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