CAS: 4025-71-2; 2-Phenylethanesulfonyl Chloride

该化合物是一种广泛用于有机合成和制药应用的多用途灭蚁灵试剂,其主要优点包括:对核糖核素具有高度反应性,能够有效地将全氟辛烷磺酸功能组引入目标分子;该化合物在酸改变,交叉结合反应和作为生产磺酰胺的中间体方面特别宝贵;其芳香联苯组在保持反应的同时,增强稳定性,使其适合在受控条件下进行选择性变异;该试剂通常在无水条件下处理,以防止水解;其定义明确的再活动特征和与各种子体的兼容性使合成化学家成为可靠的选择.

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CAS号4410-99-5 2-苯乙硫醇 | CAS号6326-49-4 phenethylsulfan... | CAS号13552-93-7 2-phenylethanes... | CAS号34372-24-2 phenethylsulfan... | CAS号103-63-9 β-溴苯乙烷 | CAS号24521-57-1 S-phenethyl-iso... | CAS号28868-76-0 氯代丙二酸二甲酯 | CAS号60-12-8 苯乙醇 | CAS号5654-72-8 2-phenylethyl t... | CAS号14315-13-0 2,3-二氢苯并[b]噻吩1,... | CAS号622-24-2 β-氯代苯乙烷 | CAS号13657-49-3 1,1'-(2-Butene-... | CAS号95339-74-5 N-methyl-2-phen... | CAS号54664-50-5 Benzeneethanesu...

合成工艺路线路线简述

    📜乙基溴苯置于盐酸,N-氯代丁二酰亚胺体系中,用 N,N-二甲基甲酰胺,乙腈 作为反应溶剂,化学反应 2.0H,反应生成 2-苯基-乙烷磺酰氯
    参考文献:走向均匀的碘催化:可见光下芳烃的分子内ch胺化反应
    标题:走向均匀的碘催化:可见光下芳烃的分子内ch胺化反应
    摘要:提出了芳烃的光化学催化胺化.该反应在良性碘催化下在可见光作为引发剂的情况下进行,并提供了一系列不同取代的芳基胺的通道.总共29个实例证明了这种轻度氧化方法的广泛适用性.反应的范围可以进一步扩展到甲硅烷基系的衍生物,这些衍生物在形成七元杂环后会进行分子内胺化.硅系链的裂解提供了进入相应的3-取代苯胺的通道.
    DOI:10.1002/chem.201602138

    海关参考信息

    专利信息


    专利号:US-9422244-B2
    优先权日:2010-01-29
    标 题 :Synthesis of substituted pyrazoline carboxamidine derivatives
    发明人:VAN LOEVEZIJN ARNOLD; LANGE JOSEPHUS H M; BARF GERRIT A; DEN HARTOG ARNOLD P
    权利人:VAN LOEVEZIJN ARNOLD; LANGE JOSEPHUS H M; BARF GERRIT A; DEN HARTOG ARNOLD P; ABBVIE BAHAMAS LTD
    摘要:This invention relates to organic chemistry, in particular to processes for the preparation of pyrazoline carboxamidine derivatives of formula (I), known as potent 5-HT6 antagonists. The invention also relates to novel intermediates of these compounds. wherein the symbols have the meanings given in the description.

    专利号:EP-1836163-B1
    优先权日:2004-12-23
    标题 :Pyrrolidine derivatives for the treatment of a disease depending on the activity of renin
    发明人:BREITENSTEIN WERNER; COTTENS SYLVAIN; EHRHARDT CLAUS; JACOBY EDGAR; LORTHIOIS EDWIGE LILIANE JEANNE; MAIBAUM JUERGEN KLAUS; OSTERMANN NILS; SELLNER HOLGER; SIMIC OLIVER
    权利人:NOVARTIS AG
    摘要:Novel 3-mono-, 3,4-di- and 3,4,4,-tri-substituted pyrrolidine 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 inappropriate 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 inappropriate activity of renin; the use of a compound of that class in the treatment of a disease that depends on inappropriate activity of renin; pharmaceutical formulations comprising a said substituted pyrrolidine compound, and/or a method of treatment comprising administering a said substituted pyrrolidine compound, a method for the manufacture of said substituted pyrrolidine compounds, and novel intermediates and partial steps for their synthesis are described. The substituted pyrrolidine compounds are especially of the formula I wherein the substituents are as described in the specification.

    专利号:RU-2182904-C2
    优先权日:1996-02-09
    标题:Sulfonamides and methods of their synthesis

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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:Łyżwa, P., Science of Synthesis Knowledge Updates, (2011) 2, 490.
    摘要:Łyżwa, P., Science of Synthesis Knowledge Updates, (2011) 2, 480.
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