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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013644Generated: November 2, 2026

Ammonia → 7-Chlorothieno[3,2-b]pyridine-2-carboxamide

https://huagongshe.com/reaction/1013644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantDichloromethaneHCID 6344—
ReactantOxalyl chlorideHCID 65578—
ReactantLithium 7-chlorothieno[3,2-b]pyridine-2-carboxylateHCID 23677819—
SolventDimethylformamideHCID 6228—
Product7-Chlorothieno[3,2-b]pyridine-2-carboxamideHCID 59427281—

Reaction Steps

A 250 mL flask was charged with lithium 7-chlorothieno[3,2-b]pyridine-2-carboxylate (3.00 g, 13.7 mmol) and CH2Cl2(100 ml) under nitrogen. DMF (cat) (0.100 ml) and oxalyl dichloride (1.49 ml, 17.1 mmol) were added dropwise, and the reaction mixture was stirred for 3 hours, and concentrated in vacuo. The brown solid was redissolved in CH2Cl2(100 ml) and ammonia (gas) (0.233 g, 13.7 mmol) was gently bubbled through the reaction mixture for 5 minutes. The flask was then capped and stirred at room temperature overnight under closed atmosphere. The brown suspension was concentrated in vacuo and the resulting solid was taken up in water (to dissolve the starting material), then collected by filtration to give 7-chlorothieno[3,2-b]pyridine-2-carboxamide. MS m/z=213 [M+H]+. Calc'd for C8H5ClN25OS: 212.66.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981891B2
Source datasetuspto-grants-2011_07
ORD IDord-e48db7d95fb44711a70b2edcf84ec837
Source noteuspto-grants-2011_07