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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664884Generated: November 1, 2026

Triethylamine → HCID 135972971, compound

https://huagongshe.com/reaction/1664884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium CarbonateHCID 10340—
Reactant4-Nitrophenyl chloroformateHCID 82129—
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—
Reactant5-Phenyl-2-piperidin-4-YL-2,4-dihydro-[1,2,4]triazol-3-oneHCID 135627598—
SolventTetrahydrofuranHCID 8028—
ProductHCID 135972971HCID 13597297139.7%

Reaction Steps

Triethylamine (19 μL, 0.135 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 (18.8 mg, 0.045 mmol) and 4-nitrophenyl chloroformate (9.0 mg, 0.045 mmol) in tetrahydrofuran (2 mL) at 0° C. After 1 h, 5-phenyl-2-piperidin-4-yl-2,4-dihydro-3H-1,2,4-triazol-3-one (11 mg, 0.045 mmol) and triethylamine (19 μL, 0.135 mmol) were added and the mixture allowed to warm to ambient temperature. After 1 h, saturated aqueous sodium carbonate was added and the mixture was extracted with dichloromethane. The organic layer was washed with saturated aqueous sodium bicarbonate (3×), saturated brine, dried over sodium sulfate, filtered and concentrated. Purification by reverse phase HPLC (C-18, 95% water/acetonitrile→5% water/acetonitrile with 0.1% trifluoroacetic acid) gave the title compound (11 mg). MS 616.2509 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039460B2
Source datasetuspto-grants-2011_10
ORD IDord-47eba4d5b10d4882ba8a515565d1ae3b
Source noteuspto-grants-2011_10