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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989967Generated: November 1, 2026

Triethylamine → (Azetidin-1-yl)(2-bromo-1,3-thiazol-4-yl)methanone

https://huagongshe.com/reaction/1989967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant2-Bromothiazole-5-carboxylic acidHCID 2763210—
ReactantAzetidine hydrochlorideHCID 12308726—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product(Azetidin-1-yl)(2-bromo-1,3-thiazol-4-yl)methanoneHCID 5362965255.9%

Reaction Steps

To a solution of 2-bromothiazole-5-carboxylic acid (752 mg, 3.62 mmol) in DCM (10 mL) was slowly added oxalyl chloride (0.38 mL, 4.34 mmol) and then DMF (1 drop). The mixture was stirred for 4 hours, following which the organics were removed in vacuo, and the residues azeotroped with toluene (10 mL). The crude material was dissolved in DCM (10 mL) and slowly added to a stirred suspension of azetidine hydrochloride (404 mg, 4.34 mmol) and triethylamine (1.8 mL, 13 mmol) in DCM (25 mL). The mixture was stirred at RT for 2 hours before the organics were removed in vacuo. The residue was partitioned between ethyl acetate (50 mL) and water (25 mL), the organic layer washed with brine (25 mL), dried (MgSO4) and evaporated to a residue which was chromatographed on silica, eluting with 40% ethyl acetate in iso-hexane, to give the desired compound (500 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642263B2
Source datasetuspto-grants-2010_01
ORD IDord-ead821ffdd334d788a5956d143d6600b
Source noteuspto-grants-2010_01