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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500806Generated: October 31, 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/500806

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 numberUS07772247B2
Source datasetuspto-grants-2010_08
ORD IDord-dbbd258178b64b4fa32e569af74ad0f1
Source noteuspto-grants-2010_08