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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725661Generated: November 3, 2026

Triethylamine → HCID 11432505, compound

https://huagongshe.com/reaction/1725661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Nitrophenyl chloroformateHCID 82129—
Reactant(3R,6S)-3-Amino-6-(2,3-difluorophenyl)-1-(2,2,2-trifluoroethyl)azepan-2-oneHCID 23653826—
ReactantHCID 57562526HCID 57562526—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11432505HCID 1143250554.7%

Reaction Steps

Triethylamine (11.5 mg, 0.104 mmol) was added to a solution (3R,6S)-3-amino-6-(2,3-difluorophenyl)-1-(2,2,2-trifluoroethyl)azepan-2-one (32 mg, 0.104 mmol) and p-nitrophenyl chloroformate (20 mg, 0.104 mmol) in tetrahydrofuran (1 mL) at 0° C. After 0.5 h, triethylamine (42 mg, 10.416 mmol) and 4-piperidin-4-ylpyridazin-3(2H)-one (19 mg, 0.104 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 (1% methanol/dichloromethane→10% methanol/dichloromethane) gave the title compound (30 mg). MS 528.1999 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491713B2
Source datasetuspto-grants-2009_02
ORD IDord-44f60fccc12c487ab00aafddaba687df
Source noteuspto-grants-2009_02