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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261245Generated: November 1, 2026

7-Chlorothieno[3,2-B]pyridine-2-carbonitrile → 7-(2-Fluoro-4-nitrophenoxy)thieno[3,2-b]pyridine-2-carbonitrile

https://huagongshe.com/reaction/1261245

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Chlorothieno[3,2-B]pyridine-2-carbonitrileHCID 22278636—
Reactant7-(2-Fluoro-4-nitrophenoxy)-2-(thiazol-2-yl)thieno[3,2-b]pyridineHCID 59424425—
Product7-(2-Fluoro-4-nitrophenoxy)thieno[3,2-b]pyridine-2-carbonitrileHCID 59424421—

Reaction Steps

Following the procedure described above for the synthesis of compound 11 (example 12, step 3, scheme 2) but substituting compound 10 for compound 126, title compound 127 was obtained as a yellow solid (114 mg, 60% yield). MS (m/z) 316.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470850B2
Source datasetuspto-grants-2013_06
ORD IDord-8cea1ed287ad4062825bdbdf9a29b788
Source noteuspto-grants-2013_06