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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415905Generated: October 26, 2026

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

https://huagongshe.com/reaction/415905

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 numberUS08088794B2
Source datasetuspto-grants-2012_01
ORD IDord-4b8ebae095054f1e85807f5a7912756f
Source noteuspto-grants-2012_01