Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 1204-1210 |
| Number of pages | 7 |
| Journal | Bulletin of the Korean Chemical Society |
| Volume | 37 |
| Issue number | 8 |
| DOIs | |
| State | Published - 1 Aug 2016 |
Keywords
- Fluorescence
- Fluorous
- Small molecule microarray
- Solid-phase extraction
- Tag
- Thienopyridinone
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