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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261280Generated: November 2, 2026

4-Nitrophenol → 2-Bromo-7-(4-nitrophenoxy)thieno[3,2-b]pyridine

https://huagongshe.com/reaction/1261280

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
Reactant2-Bromo-7-chlorothieno[3,2-b]pyridineHCID 18382774—
Reactant2-Bromo-7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridineHCID 59424521—
Product2-Bromo-7-(4-nitrophenoxy)thieno[3,2-b]pyridineHCID 5942446148%

Reaction Steps

Starting from the compound 41 (scheme 8) and following the procedure described above for the synthesis of compound 42 (scheme 8) but replacing 2-fluoro-4-nitrophenol for 4-nitrophenol, title compound 197 was obtained in 48% yield. LRMS (M+1) 350.9 (100%). 352.9 (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470850B2
Source datasetuspto-grants-2013_06
ORD IDord-db8b456311574a7e9a31e1156b71b42a
Source noteuspto-grants-2013_06