Synthesis of Tetrasubstituted Thieno[3,2-b]pyridin-5(4H)-one Derivatives as a Heterocyclic Scaffold for Multisite-specific Fluorous Fluorescent Tagging and Fluorous Solid-Phase Extraction

被引:0
|
作者
Jeon, Moon-Kook [1 ]
Yi, Su-Jin [1 ,2 ]
Son, Seung Uk [2 ]
机构
[1] Korea Res Inst Chem Technol, Bio & Drug Discovery Div, Med Chem Res Ctr, Daejeon 305600, South Korea
[2] Sungkyunkwan Univ, Dept Chem, Suwon 440746, South Korea
来源
关键词
Small molecule microarray; Tag; Fluorous; Fluorescence; Thienopyridinone; Solid-phase extraction; SMALL-MOLECULE MICROARRAYS; ANTAGONISTS; INHIBITORS; RECEPTOR; TECHNOLOGIES; DISCOVERY; PEPTIDE; BINDING; POTENT; DRUGS;
D O I
10.1002/bkcs.10840
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Tetrasubstituted thieno[3,2-b]pyridin-5(4H)-one derivatives were selected as a highly functionalized heterocyclic scaffold for a multisite-specific tagging process utilizing a previously devised fluorous fluorescent tag system. A suitable synthetic method was established for the 7-alkoxy-2,4,6-trisubstituted-thieno[3,2-b]pyridin-5(4H)-one derivatives, and incorporating t-butoxycarbonyl-functionalized building blocks into the reaction sequence produced precursors that could be used in the tagging process. Fluorous solid-phase extraction facilitated the purification of the tagged target compounds after a series of reactions, including t-Bu deprotection/N-hydroxysuccinimidyl ester formation/amidation.
引用
收藏
页码:1204 / 1210
页数:7
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