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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725660Generated: November 1, 2026

Triethylamine → HCID 11341141, compound

https://huagongshe.com/reaction/1725660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Nitrophenyl chloroformateHCID 82129—
Reactant1-Piperidin-4-ylimidazolidine-2,4-dioneHCID 57428923—
Reactant(3R,6S)-3-Amino-6-(2,3-difluorophenyl)-1-(2-methoxyethyl)azepan-2-oneHCID 60037873—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11341141HCID 1134114121.1%

Reaction Steps

Triethylamine (0.012 mL, 0.084 mmol) was added to a solution (3R,6S)-3-amino-6-(2,3-difluorophenyl)-1-(2-methoxyethyl)azepan-2-one (25 mg, 0.084 mmol) and p-nitrophenyl chloroformate (25 mg, 0.126 mmol) in tetrahydrofuran (1 mL) at 0° C. After 0.5 h, triethylamine (0.036 mL, 0.252 mmol) and 1-piperidin-4-ylimidazolidine-2,4-dione (23 mg, 0.126 mmol) were added and the mixture was allowed to warm to ambient temperature. After 1 h, the mixture was quenched with water, extracted with ethyl acetate, and washed with 1 N NaOH solution. The combined organic layer was dried over sodium sulfate, filtered, and concentrated. Purification by silica gel chromatography (0.5% methanol/dichloromethane→7% methanol/dichloromethane) gave the title compound (9 mg). MS 508.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491713B2
Source datasetuspto-grants-2009_02
ORD IDord-7247361675a847babdbeae88b93a52af
Source noteuspto-grants-2009_02