CAS: 41840-28-2; O-Tert-Butyl S-(4,6-Dimethylpyrimidin-2-yl) Carbonothioate

该化合物是属于硫酯类的有机化合物.该物质具有碳酰胺功能组,其特点是硫磺原子与碳基碳结合,其特点是碳酰胺元素存在一个碳酰亚酸酯;该化合物具有与氧原子相连的分支烷基(1,1-二甲基乙基)组,有助于其消毒特性.此外,该化合物在4和6个位置上含有一个以两组甲基组替代的铁酰胺环,可影响其生物活动和溶性.这些功能组的存在表明,由于经常与硫酰胺衍生物相关的生物活动,有可能在农业化学中应用,特别是农药或除草剂.该化合物的稳定性,再活性和与其他物质的相互作用可能受到其分子结构的影响,从而在合成化学和应用化学环境中都引起兴趣.

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    专利信息


    专利号:WO-2025027521-A1
    优先权日:2023-08-01
    标题 :An improved process for the preparation of avibactam and intermediate thereof
    发明人:DHAVARIA SANDEEP; HANDA VISHAL; SHARMA SUNEEL KUMAR; MEHTA ANSHU KUMAR; SINGH ADITYA NARAYAN; ABUL AZIM; GUPTA NITIN; SINGH GOVIND; CABRI WALTER
    权利人:FRESENIUS KABI ONCOLOGY LTD
    摘要:The present invention relates to an improved process for the preparation of Avibactam or a pharmaceutically acceptable salt thereof, particularly the present invention relates to process for the preparation of a bridged ester intermediate of Formula I, wherein R1 is a hydroxy protecting group which is a key intermediate for Avibactam or a pharmaceutically acceptable salt thereof. The present invention also relates to the crystalline form of intermediates used for the synthesis of Avibactam or a pharmaceutically acceptable salt thereof. The invention also provides improved processes for the preparation of Avibactam or a pharmaceutically acceptable salt, using the bridged ester compound of formula I prepared by the process of the present invention.

    专利号:US-4337336-A
    优先权日:1980-02-25
    标 题:Derivative of kanamycin A and a process for the preparation thereof
    发明人:UMEZAWA HAMAO; UMEZAWA SUMIO; FUKATSU SHUNZO; YONETA TOSHIO; WAKAZAWA TADASHI
    权利人:MICROBIAL CHEM RES FOUND
    摘要:There are provided new compounds, 3',4'-anhydro-4'-epi derivatives of kanamycin A of the formula: ##STR1## wherein R represents an alkyl, aralkyl or aryl group and Y represents an alkylidene, aralkylidene, cycloalkylidene or tetrahydropyranylidene group which are useful as an intermediate for the synthesis of 3',4'-dideoxykanamycin A and 4'-deoxykanamycin A from kanamycin A. The compounds of formula (I) can be prepared by treating the corresponding 4'-O-sulfonyl derivative with an alkali metal alcoholate in a lower alkanol under an alkaline condition.

    专利号:US-12122769-B2
    优先权日:2017-10-19
    标题 :Synthesis of antibacterial aminoglycoside analogs
    发明人:TREND RAISSA; DAPPEN MICHAEL; HENRY CHRISTOPHER E; GOLDBLUM ADAM AARON; AGGEN JAMES BRADLEY; MENDONÇA RICARDO FILIPE DE JESUS GONÇALVES; SARDINHA JOÃO CARLOS FALCÃO
    权利人:CIPLA USA INC
    摘要:The present disclosure relates to novel methods for preparing antibacterial aminoglycoside compounds, as well as to related intermediates, and crystal forms thereof, useful in such methods.

    专利号:AU-2022253019-A1
    优先权日:2021-04-09
    标题:Synthesis of rapamycin analog compounds

    专利号:EP-3697797-A1
    优先权日:2017-10-19
    标题 :Synthesis of antibacterial aminoglycoside analogs

    专利号:CN-111655709-A
    优先权日:2017-10-19
    标 题:Synthesis of Antibacterial Aminoglycoside Analogs

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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).
    摘要:Lipton, M. F.; Mauragis, M. A., Science of Synthesis, (2005) 21, 554.
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