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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588833Generated: November 2, 2026

Triethylamine → HCID 90460107, compound

https://huagongshe.com/reaction/588833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
ReactantHCID 90460454HCID 90460454—
SolventDichloromethaneHCID 6344—
SolventHydrochloride methanolHCID 21893726—
ProductHCID 90460107HCID 9046010782%

Reaction Steps

A mixture of tert-butyl 3-(4-(4,5-dichloro-2-methoxybenzylcarbamoyl)piperidin-1-yl)azetidine-1-carboxylate (210 mg, 0.44 mmol) in HCl/MeOH (10 mL, 2.86 M) was stirred at room temperature for 1 h. The mixture was concentrated in vacuo to yield the crude residue. The residue was dissolved in DCM (5 mL), triethylamine (0.5 mL) and acryloyl chloride (40 mg, 0.43 mmol) were added. The reaction mixture was stirred at room temperature for 30 min and then partitioned between DCM and water. The organic layer was washed with water and brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel (dichloromethane/methanol=50:1) to afford the desired product (150 mg, 82% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227978B2
Source datasetuspto-grants-2016_01
ORD IDord-10569a0444254330b226ac94496e4ab1
Source noteuspto-grants-2016_01