CAS: 10160-87-9; 3,3-Diethoxyprop-1-Yne

该化合物是一种多用途化学中间体,主要用于有机合成;其乙烷功能在基本和中性条件下保持稳定,同时在酸性水解下保持反应性,有助于在多步反应中保护甲醛群体;该丙烯二烯二乙烷为点击化学,循环添加剂和其他以烷基为基础的变异提供了额外的再活性;该化合物在制药和农用化学研究中特别宝贵,需要选择性地去防护和进一步功能化;其室温下的液体形式确保实验室环境中的处理方便;由于对水分和酸环境的敏感性,应注意将其储存在惰性条件下.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

Propargylic aldehyde ethanol 2,2-dibromo-propionaldehyde diethylacetal 6,6-diethoxy-3-methyl-hex-4-yn-3-ol1,3,3-triethoxypropene 4'-(pyrimidin-2-ylsulfamoyl)acetanilide 2-methylpyrimidine 1-phenylpyrazole

合成工艺路线路线简述

    Alkaline Earth Salt Of/the/ Methylsulfuric Acid置于氢氧化钾体系中,化学反应生成丙醛二乙基乙缩醛
    参考文献:Sheehan; Robinson,Journal Of The American Chemical Society,1949,Vol. 71,P. 1436,1438
    标题:Sheehan; Robinson,Journal Of The American Chemical Society,1949,Vol. 71,P. 1436,1438

    专利信息


    专利号:US-2016257688-A1
    优先权日:2013-10-24
    标 题 :Process for Synthesis of Lactams
    发明人:TAVARES FRANCIS XAVIER
    权利人:TAVARES FRANCIS XAVIER
    摘要:Methods for the synthesis of lactams are presented whereby a carboxylic acid of the formula HOOC—OR—NH-LG, wherein OR is an organic moiety and LG is a leaving group, is reacted with an acid, such as an organic acid, in particular a strong acid, and a dehydrating agent, which may be one in the same such as a strong acid anhydride, such that the amount of acid added allows for the desired transformation to take place without the loss of the leaving group (LG) before the cyclization, and recovering the lactam such as that of the formula (a), provided herein, wherein G represents the atom(s) needed to form a closed ring.

    专利号:US-7109377-B2
    优先权日:1996-10-16
    标 题:Synthesis of combinatorial libraries of compounds reminiscent of natural products
    发明人:SCHREIBER STUART L; SHAIR MATTHEW D; TAN DEREK S; FOLEY MICHAEL A; STOCKWELL BRENT R
    权利人:HARVARD COLLEGE
    摘要:The present invention provides complex compounds reminiscent of natural products and libraries thereof, as well as methods for their production. The inventive compounds and libraries of compounds are reminiscent of natural products in that they contain one or more stereocenters, and a high density and diversity of functionality. In general, the inventive libraries are synthesized from diversifiable scaffold structures, which are synthesized from readily available or easily synthesizable template structures. In certain embodiments, the inventive compounds and libraries are generated from diversifiable scaffolds synthesized from a shikimic acid based epoxyol template. In other embodiments, the inventive compounds and libraries are generated from diversifiable scaffolds synthesized from the pyridine-based template isonicotinamide. The present invention also provides a novel ortho-nitrobenzyl photolinker and a method for its synthesis. Furthermore, the present invention provides methods and kits for determining one or more biological activities of members of the inventive libraries. Additionally, the present invention provides pharmaceutical compositions containing one or more library members.

    专利号:WO-2024116069-A1
    优先权日:2022-11-28
    标题 :Novel trilaciclib intermediates, method of preparation and use thereof
    发明人:KADU Rushikesh Vilasrao; RENGASAMY VADIVELANV; SINGH SATNAM; SHARMA SUBRAMANYA; DAUND VAIBHAV SURESH; KUSHWAHA SANDEEP; LAL KANHAIYA; YAZALI VENKATA SUBBARAO
    权利人:ASSIA CHEM IND LTD
    摘要:Aspects of the present disclosure provide novel intermediates that may be used for synthesis of Trilaciclib, pharmaceutically acceptable salts or derivatives thereof. Aspects of the present disclosure also relate to a method for preparation of Trilaciclib intermediates. Further aspects of the present disclosure relate to method for preparation of Trilaciclib, pharmaceutically acceptable salts and derivatives thereof. Still further aspects of the present disclosure are drawn towards use of the Trilaciclib intermediates for the production of Trilaciclib, pharmaceutically acceptable salts or derivatives thereof.

    专利号:US-11465997-B2
    优先权日:2017-06-22
    标 题 :Synthesis of disorazoles and analogs thereof as potent anticancer agents
    发明人:NICOLAOU KYRIACOS C; BELLAVANCE GABRIEL; BUCHMAN MAREK; PULUKURI KIRAN KUMAR; RIGOL STEPHAN
    权利人:UNIV RICE WILLIAM M
    摘要:In one aspect, the present disclosure provides disorazole analogs of the formula: Formula (I) wherein the variables are as defined herein. In another aspect, the present disclosure also provides methods of preparing the compounds disclosed herein. In another aspect, the present disclosure also provides pharmaceutical compositions and methods of use of the compounds disclosed herein. Additionally, drug conjugates with cell targeting moieties of the compounds are also provided.

    专利号:US-2003082830-A1
    优先权日:1996-10-16
    标 题:Synthesis of combinatorial libraries of compounds reminiscent of natural products

    专利号:WO-0006525-A9
    优先权日:1998-07-25
    标题:Synthesis of combinatorial libraries of compounds reminiscent of natural products
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    合成参考文献


    摘要:Baird, M. S., Science of Synthesis, (2010) 47, 1111.
    摘要:Mérour, J.-Y.; Joseph, B., Science of Synthesis Knowledge Updates, (2016) 3, 92.
    摘要:Mérour, J.-Y.; Joseph, B., Science of Synthesis Knowledge Updates, (2016) 3, 263.
    摘要:Götzinger, A. C.; Müller, T. J. J., Science of Synthesis Knowledge Updates, (2017) 3, 16.
    摘要:Merino, P., Science of Synthesis Knowledge Updates, (2010) 4, 363.
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