CAS: 16182-15-3; 2,4,6-Trimethylbenzenesulfonohydrazide

该化合物是一种专门有机化合物,主要用作合成化学应用中的磺酰胺衍生物,其主要优点包括它作为多用途中间体,在生产对有机合成,特别是形成碳-碳和碳-乙氧环具有价值的磺酰亚氮化物方面发挥着有益作用.该化合物的三甲基替代芳香环增强了其稳定性和再活动性,使其适合受控分解反应,如聚合化学中的泡沫或交叉连接剂.其明确界定的结构确保了需要精确的磺酰胺前体的反应的一贯性能.该化合物由于对湿度和热度的敏感性,通常在受控条件下处理.

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39085-59-1 4543-58-2 18626-10-3

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CAS号38202-27-6 O-(2,4,6-三甲基苯磺酰... | CAS号773-64-8 2,4,6-三甲基苯磺酰氯 | CAS号3112-82-1 Benzene,1,3,5-t... | CAS号111708-96-4 1,3,5-trimethyl... | CAS号83477-71-8 N'-Cyclopentyli... | CAS号85487-86-1 N-[(2-bromo-1-p...

合成工艺路线路线简述

    📜O-(2,4,6-三甲基苯磺酰基)乙酰羟肟酸乙酯置于高氯酸体系中,用 1,4-二氧六环,水 用作溶剂,化学反应 7.5H,反应生成2,4,6-三甲基苯磺酰肼
    参考文献:N-Aryl-2-Oxazolidinone-5-Carboxamides And Their Derivatives
    标题:N-Aryl-2-Oxazolidinone-5-Carboxamides And Their Derivatives
    摘要:本发明提供了具有以下式i,Ii和iii的抗菌剂.

    海关参考信息

    专利信息


    专利号:US-9783549-B2
    优先权日:2013-11-04
    标题:Macrocyclization reactions and intermediates useful in the synthesis of analogs of halichondrin B
    发明人:FANG FRANCIS G; KIM DAE-SHIK; CHOI HYEONG-WOOK; CHASE CHARLES E; LEE JAEMOON
    权利人:EISAI R&D MAN CO LTD
    摘要:The invention provides methods for the synthesis of eribulin or a pharmaceutically acceptable salt thereof (e.g., eribulin mesylate) through a macrocyclization strategy. The macrocyclization strategy of the present invention involves subjecting a non-macrocyclic intermediate to a carbon-carbon bond-forming reaction (e.g., an olefination reaction (e.g., Homer-Wadsworth-Emmons olefination), Dieckmann reaction, catalytic Ring-Closing Olefin Metathesis, or Nozaki-Hiyama-Kishi reaction) to afford a macrocyclic intermediate. The invention also provides compounds useful as intermediates in the synthesis of eribulin or a pharmaceutically acceptable salt thereof and methods for preparing the same.

    专利号:US-2014011992-A1
    优先权日:2012-12-20
    标 题:Synthesis of abiraterone and related compounds
    发明人:PEREZ ENCABO ALFONSO; TURIEL HERNANDEZ JOSE ANGEL; GALLO NIETO FRANCISCO JAVIER; LORENTE BONDE-LARSEN ANTONIO; SANDOVAL RODRIGUEZ CELSO MIGUEL
    权利人:CRYSTAL PHARMA SAU
    摘要:The present invention relates to processes for obtaining abiraterone and derivatives thereof, such as abiraterone acetate, by means of a Suzuki coupling through a steroid borate of general formula (IV) or a C—C coupling through a steroid hydrazone of general formula (II), as well as to intermediates useful in said processes.

    专利号:WO-2022170218-A1
    优先权日:2021-02-05
    标题:Intramolecular cyclization for general synthesis of bicyclic alkyl bioisostere boronates
    发明人:QIN TIAN; YANG YANGYANG; TSIEN JET
    权利人:UNIV TEXAS
    摘要:Disclosed herein are methods of synthesizing compounds of the formula (I) wherein the variables are defined herein. Also provided are compounds produced using these methods. In some aspects, the methods provided herein may be used to install aryl bioisosteres.

    专利号:US-2019144463-A1
    优先权日:2013-11-04
    标题:Macrocyclization reactions and intermediates and other fragments useful in the synthesis of analogs of halichondrin b

    专利号:US-11643418-B2
    优先权日:2013-11-04
    标题:Macrocyclization reactions and intermediates and other fragments useful in the synthesis of analogs of halichondrin B

    专利号:US-10934307-B2
    优先权日:2013-11-04
    标题 :Macrocyclization reactions and intermediates and other fragments useful in the synthesis of analogs of halichondrin B

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献

    [参考文献]: Mario Uosis-Martin, Et Al. A Model System For The Synthesis Of Complanadine Alkaloids By "Diverted Kondrat'Eva" Oxazole-Olefin Cycloaddition. J Org Chem. 2013 Jun 21;78(12):6253-63.

    合成参考文献


    摘要:Kwiatkowska, M.; Kiełbasiński, P., Science of Synthesis: Knowledge Updates, (2024) 3, 437.
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