CAS: 23138-50-3; 1-Ethyl-4-Isocyanatobenzene

上下游产品

bis(trichloromethyl) carbonate 4-aminoethylbenzene ethyl 2-hydroxy-3-methyl-3-butenoate 2'-amino-4-ethylbiphenyl 1-(4-Ethyl-phenyl)-3-(1-methyl-1-phenyl-ethyl)-urea (4-Ethyl-phenyl)-carbamic acid 2-piperidin-1-yl-ethyl ester; hydr°Chloride (4-ethyl-phenyl)-carbamic acid 2-(4-dibenzylsulfamoyl-phenyl)-2-oxo-ethyl ester

三光气,4-乙基苯胺 以 二氯甲烷 用作溶剂,化学反应 0.5H,反应生成4-乙基苯基异氰酸酯
参考文献:三乙胺还原中间体异氰酸酯简单高效合成二芳基脲
标题:三乙胺还原中间体异氰酸酯简单高效合成二芳基脲
摘要:从芳胺和三光气以三乙胺作为中间体异氰酸酯的还原剂合成了三十种对称的二芳基脲衍生物,收率中等至极好.重要的是,部分产物可以在没有柱色谱的情况下以几乎定量的收率收集.在温和的反应条件下,该过程可以容忍广泛的官能团.化合物的结构通过NMR,Ms和x-射线晶体学分析确定.
Doi:10.3184/174751913X13663925002708

专利信息

专利号:US-9879050-B2
优先权日:2013-08-30
标 题 :Substituted urea depsipeptide analogs as activators of the CLPP endopeptidase
发明人：LEE RICHARD E; ZHAO YING; GRIFFITH ELIZABETH; ZHENG ZHONG; SINGH AMAN P
权利人:ST JUDE CHILDREN'S RES HOSPITAL
摘要:In one aspect, the invention relates to substituted urea depsipeptide analogs, derivatives thereof, and related compounds, which are useful as activators the ClpP endopeptidease; synthesis methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating infectious disease using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

专利号:CN-111471171-B
优先权日:2019-01-24
标 题:A kind of aryl sulfonic acid intermediate and its preparation method, and its application for the synthesis of low temperature sensitive admixture for concrete

专利号:US-10570179-B2
优先权日:2016-09-02
标 题:Substituted urea depsipeptide analogs as activators of the CLPP endopeptidase
发明人：LEE RICHARD E; ZHAO YING
权利人:ST JUDE CHILDRENS RES HOSPITAL
摘要:In one aspect, the invention relates to substituted urea depsipeptide analogs, derivatives thereof, and related compounds, which are useful as activators the ClpP endopeptidease; synthesis methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating infectious disease using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

专利号:US-10822377-B2
优先权日:2015-03-04
标 题:Substituted urea depsipeptide analogs as activators of the ClpP endopeptidase
发明人：LEE RICHARD E; ZHAO YING; JIUYU LIU
权利人:ST JUDE CHILDRENS RES HOSPITAL
摘要:In one aspect, the invention relates to substituted urea depsipeptide analogs, derivatives thereof, and related compounds, which are useful as activators the ClpP endopeptidease; synthesis methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating infectious disease using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

专利号:EP-0789577-A1
优先权日:1995-06-07
标 题:Synthesis of n-substituted oligomers

专利号:WO-9640202-A1
优先权日:1995-06-07
标 题:Synthesis of n-substituted oligomers