Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710946Generated: November 2, 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/1710946

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 numberUS07790729B2
Source datasetuspto-grants-2010_09
ORD IDord-b3d969946d6e4ec48037b930e24c4df6
Source noteuspto-grants-2010_09