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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173028Generated: October 30, 2026

7-Chlorothieno[3,2-b]pyridine → Thienopyridine

https://huagongshe.com/reaction/2173028

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Chlorothieno[3,2-b]pyridineHCID 11275251—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
ProductThienopyridineHCID 12210218—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 7-chlorothieno[3,2-b]pyridine (500 mg, 2.95 mmol) and zinc (193 mg, 2.95 mmol) in acetic acid (5 mL) was stirred at room temperature for 3 days, followed by stirring at 50° C. for 5 hours. The solvent was removed in vacuo and the residue was dissolved in DCM (200 mL) and extracted with 1N NaOH (500 mL). The aqueous layer was washed again with DCM (2×200 mL). The organic layers were combined, dried over Na2SO4, and the solvent was removed in vacuo to yield the title compound as a yellow oil, which was used without further purification. ESI-MS m/z [M+H]+ calc'd for C7H5NS, 136. found, 136.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056873B2
Source datasetuspto-grants-2015_06
ORD IDord-86ad34e6e52c496790c3b2e5be429d45
Source noteuspto-grants-2015_06