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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600554Generated: October 29, 2026

Triethylamine → (Azetidin-1-yl)(5-chloropyrazin-2-yl)methanone

https://huagongshe.com/reaction/600554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAzetidineHCID 10422—
ReactantOxalyl chlorideHCID 65578—
Reactant5-Chloropyrazinoic acidHCID 465472—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product(Azetidin-1-yl)(5-chloropyrazin-2-yl)methanoneHCID 4687032882%

Reaction Steps

Oxalyl chloride (1.55 mL, 17.5 mmol), followed by DMF (2 drops), was added to a mixture of 5-chloropyrazine-2-carboxylic acid (CAS no. 36070-80-1, Intermediate 33) (2.31 g, 14.6 mmol) in DCM (40 mL). The reaction was stirred at RT for 2 hours after which time the volatiles were removed under reduced pressure. The residue was taken up DCM (40 mL) and azetidine (1.08 mL, 16.03 mmol) and triethylamine (4.46 mL, 32.06 mmol) added. The mixture was stirred at RT for 72 hours. The volatiles were removed under reduced pressure and ethyl acetate (100 mL) added to the residue. The organics were washed with water (100 mL), citric acid (50 mL), saturated sodium bicarbonate solution (50 mL) and brine (50 mL), dried (MgSO4), filtered and the solvent removed under reduced pressure. The residue was purified by flash chromatography, eluting with a gradient of 50-100% ethyl acetate in isohexane, to afford the product (2.38 g, 82%). 1HNMR δ (400 MHZ, CDCl3): 2.35-2.42 (2H, m), 4.26 (2H, t), 4.67 (2H, t), 8.52 (1H, d), 9.09 (1H, d); m/z 198 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902200B2
Source datasetuspto-grants-2011_03
ORD IDord-922187e9d99d4b4b9e514ffc12b3b231
Source noteuspto-grants-2011_03