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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664908Generated: October 31, 2026

Triethylamine → HCID 59722573, compound

https://huagongshe.com/reaction/1664908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium CarbonateHCID 10340—
Reactant4-Nitrophenyl chloroformateHCID 82129—
ReactantHCID 59722552HCID 59722552—
Reactant(6S,9R)-6-(2,3-difluorophenyl)-3-(2,2,2-trifluoroethyl)-6,7,8,9-tetrahydro-5H-imidazo[1,2-a]azepin-9-amineHCID 67438873—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59722573HCID 5972257343.9%

Reaction Steps

Triethylamine (33 μL, 0.24 mmol) was added to a solution of the hydrochloride salt of (6S,9R)-6-(2,3-difluorophenyl)-3-(2,2,2-trifluoroethyl)-6,7,8,9-tetrahydro-5H-imidazo[1,2-a]azepin-9-amine (33 mg, 0.08 mmol) and 4-nitrophenyl chloroformate (16 mg, 0.08 mmol) in tetrahydrofuran (1 mL) at 0° C. After 15 min, a solution of 6-phenyl-4-piperidin-4-ylpyridazin-3(2H)-one (20 mg, 0.08 mmol) in dichloromethane (1 mL) and triethylamine (22 μL, 0.16 mmol) were added and the mixture allowed to warm to ambient temperature. After 2 h, saturated aqueous sodium carbonate was added and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium bicarbonate (3×), saturated brine, dried over magnesium sulfate, filtered and concentrated. Purification by silica gel chromatography (100% dichloromethane→90% dichloromethane/methanol) gave the title compound (22 mg). MS 627.2498 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039460B2
Source datasetuspto-grants-2011_10
ORD IDord-40b616669ec54774abfd34e4d491f442
Source noteuspto-grants-2011_10