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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359690Generated: October 31, 2026

Oxalyl chloride → 2-(Azetidin-1-ylcarbonyl)-7-chlorothieno[3,2-b]pyridine

https://huagongshe.com/reaction/2359690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
ReactantAzetidine hydrochlorideHCID 12308726—
ReactantLithium 7-chlorothieno[3,2-b]pyridine-2-carboxylateHCID 23677819—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-(Azetidin-1-ylcarbonyl)-7-chlorothieno[3,2-b]pyridineHCID 22143549100.7%

Reaction Steps

A 50 mL round bottom flask was charged with lithium 7-chlorothieno[3,2-b]pyridine-2-carboxylate (0.500 g, 2.28 mmol), methylene chloride (15 ml), and 12 drops of DMF. Oxalyl chloride (0.298 ml, 3.42 mmol) was added dropwise, and the mixture was stirred at room temperature for 3 hours and concentrated to yield a tan solid. This was redissolved in methylene chloride (15 ml). Azetidine hydrochloride (0.426 g, 4.55 mmol) was added in one portion and Hunig's Base (1.59 ml, 9.11 mmol) was added dropwise. This mixture was stirred at room temperature overnight, then diluted with methylene chloride (15 mL) and washed with water (25 mL), sat. NaHCO3 (25 mL), and brine (25 mL). The organic layer was dried with MgSO4, filtered, and concentrated in vacuo to yield azetidin-1-yl(7-chlorothieno[3,2-b]pyridin-2-yl)methanone (0.58 g, 100% yield) as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685983B2
Source datasetuspto-grants-2014_04
ORD IDord-e3c54248154f42649b021545f95abc13
Source noteuspto-grants-2014_04