CAS: 66715-65-9; Pyridine-2-Sulfonyl Chloride

该化合物是一个由pyridine衍生的芳烃基磺酰氯,在2号站点,该化合物的特点是用一个环状环替换成一个环状氯基磺酸盐组,该化合物一般没有颜色,可粉色黄色液体,以其浓厚的气味闻名.Pyridine-2-sultfonyl C氯具有高度反应性,特别是由于存在可以随时参与核生殖器替代反应的全氟氯化物质组,因此该物质通常用作有机合成的试剂,特别是用于将磺酰胺组引入各种子体.此外,该化合物可以作为制药和农用化学剂的中间体.由于具有再活性,应当小心处理,因为它可能具有腐蚀性,并可能对皮肤,眼睛和呼吸系统造成刺激.在与该化合物合作时,适当的安全防范措施,包括使用个人防护设备,是不可或缺的.

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欧盟法规

C&L通报

上下游产品

2-Sulfanylpyridine hydrogenchloride chlorine 2-bromo-pyridinepyridine-2-sulfonic acid-[2]pyridylamide pyridine-2-sulfonic acid dimethylamide N-Phenylpyridine-2-sulfonamide 2-pyridinesulfonamide

合成工艺路线路线简述

  • 合成目标产物 Pyridine-2-Sulfonyl Chloride 主要起始原料 Sodium Pyridine-2-Sulfinate
  • (文献来源)合成步骤主要原料 Sodium Pyridine-2-Sulfinate
📜2,2'-二硫二吡啶置于sodium Hydrogen Sulfate,Sodium Hypochlorite Pentahydrate体系中,用87 %的收率获得产物吡啶-2-磺酰氯
参考文献:通过可伸缩,环保且经济高效的工艺机械合成磺酰胺
标题:通过可伸缩,环保且经济高效的工艺机械合成磺酰胺
摘要:在此,我们展示了一种无溶剂机械化学方法,涉及由固体次氯酸钠(naocl.5H2O)介导的一锅双步程序,用于合成磺酰胺.该方案需要在催化固体酸性物质存在下对二硫化物进行串联氧化氯化反应,然后在路易斯酸碱固体无机试剂的促进下进行胺化.该方法适用于芳香族和脂肪族二硫化物和胺.纯化过程充分考虑了环境问题,避免了恶劣的条件,以获得纯净的磺酰胺产品.一些相关的生物活性化合物已经用此过程制备.
DOI:10.1039/d3Gc01894F

海关参考信息

专利信息


专利号:US-6943254-B2
优先权日:1997-03-07
标 题 :Synthesis of pyrazinyl pyridine-3-sulfonamide compounds
发明人:HOGAN PHILIP JOHN
权利人:ASTRAZENECA UK LTD
摘要:A process for the manufacture of: n n nwherein R is (1-4C)alkyl, carboxyl(1-4C)alkyl or 1,3,4-oxadiazol-2-yl comprises:n (a) reaction of the diazonium salt of 3-amino-2-chloropyridine with thionyl chloride in water and an electron transfer catalyst; (b) reaction with isobutyl-(3-methoxy-5-methylpyrazin-2-yl)carbamate and an alkali metal hydride in inert solvent; and (I) where R is (1-4C)alkyl, carboxy(1-4C)alkyl: (c) reaction with a boronic acid: n n (or an anhydride or ester therof) in the presence of a base and a palladium or nickel catalyst in solvent; and removal of the isobutoxy carbonyl group; or (ii) where R is 1,3,4-oxadiazol-2-yl (c) reaction with 4-methoxycarbonylphenylboronic acid (or an anhydride or ester thereof) with a source fluoride ion under aqueous conditions; (d) removal of the isobutoxycarbonyl protecting group; (e) conversion of the methyl ester group to the hydrazide; and (f) conversion to a 1,3,4-oxadiazol-2-yl moiety.

专利号:WO-03045909-A2
优先权日:2001-11-21
标 题 :Methods and intermediates for the synthesis of azepines

专利号:EP-0877022-A1
优先权日:1997-05-09
标 题:Synthesis of the sulfonylpyrimidine derivatives with anticancer activity

专利号:US-2008194629-A1
优先权日:2005-05-03
标题 :3-Mono-and 3,5-Disubstituted Piperidine Derivatives as Renin Inhibitors
发明人:BAESCHLIN DANIEL KASPAR; BREITENSTEIN WERNER; EHRHARDT CLAUS; MAIBAUM JUERGEN KLAUS; OSTERMANN NILS; ZIMMERMANN JUERG; RUDISSER SIMON; VANGREVELINGHE ERIC; IRIE OSAMU; UMEMURA ICHIRO; SUZUKI MASAKI; MOGI MUNETO; KANAZAWA TAKANORI; YOKOKAWA FUMIAKI; NIHONYANAGI ATSUKO
权利人:BAESCHLIN DANIEL KASPAR; BREITENSTEIN WERNER; EHRHARDT CLAUS; MAIBAUM JUERGEN KLAUS; OSTERMANN NILS; ZIMMERMANN JUERG; RUDISSER SIMON; VANGREVELINGHE ERIC; IRIE OSAMU; UMEMURA ICHIRO; SUZUKI MASAKI; MOGI MUNETO; KANAZAWA TAKANORI; YOKOKAWA FUMIAKI; NIHONYANAGI ATSUKO
摘要:The invention relates to 3,5-piperidine compounds, these compounds for use in the diagnostic and therapeutic treatment of a warm-blooded animal, especially for the treatment of a disease (=disorder) that depends on activity of renin; the use of a compound of that class for the preparation of a pharmaceutical formulation for the treatment of a disease that depends on activity of renin; the use of a compound of that class in the treatment of a disease that depends on activity of renin; pharmaceutical formulations comprising a 3,5-piperidine compound, and/or a method of treatment comprising administering a 3,5-piperidine compound, a method for the manufacture of a 3,5-piperidine compound, and novel intermediates and partial steps for their synthesis. Especially, the 3,5-piperidine compounds have the formula I, wherein the symbols have the meanings described in the specification.

专利号:US-4722749-A
优先权日:1986-06-27
标题 :Pyridinesulfonamides and their use as herbicidal agents
发明人:LEE SHY-FUH
权利人:SANDOZ LTD
摘要:Substituted 2-pyridinesulfonamide 1-oxides, synthesis thereof, intermediates therefor, and the use of said compounds for the control of weeds.

专利号:CN-106432067-A
优先权日:2016-09-18
标题 :A kind of green chemical synthesis method of 3-pyridinesulfonyl chloride

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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:One-Pot Synthesis Of Sulfonamides And Sulfonyl Azides From Thiols Using Chloramine-T
作者:Behrooz Maleki,Saba Hemmati,Reza Tayebee,Sirous Salemi,Yasaman Farokhzad,Mehdi Baghayeri,Farrokhzad Mohammadi Zonoz,Elahe Akbarzadeh,Rohollah Moradi,Azam Entezari,Mohammad Reza Abdi,Samaneh Sedigh Ashrafi,Fereshteh Taimazi,Majid Hashemi |发布日期:2013.11
摘要:A Convenient Synthesis Of Sulfonamides And Sulfonyl Azides From Thiols Is Described. In Situ Preparation Of Sulfonyl Chlorides From Thiols Was Accomplished By Oxidation With Chloramine‐t (=n‐chlorotosylamide=n‐chloro‐4‐methylbenzenesulfonamide), Tetrabutylammonium Chloride (Bu4Ncl), And H2O. The Sulfonyl Chlorides Were Then Further Allowed To React With Excess Amine Or Nan3 In The Same Pot.

合成参考文献


摘要:Shi, L., Science of Synthesis: Knowledge Updates, (2024) 1, 48.
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