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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725657Generated: October 31, 2026

Phosgene → n-[(3r,7r)-1-(Cyclopropylmethyl)-2-oxo-7-phenylazepan-3-yl]-4-(2-oxo-4-phenyl-2,3-dihydro-1h-imidazol-1-yl)piperidine-1-carboxamide

https://huagongshe.com/reaction/1725657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantDiisopropylethylamineHCID 81531—
Reactant(3R,7R)-3-Amino-1-(cyclopropylmethyl)-7-phenylazepan-2-oneHCID 58844838—
Reactant4-(2-oxo-4-phenyl-2,3-dihydro-1H-imidazol-1-yl)piperidinium chlorideHCID 67343322—
SolventDichloromethaneHCID 6344—
Productn-[(3r,7r)-1-(Cyclopropylmethyl)-2-oxo-7-phenylazepan-3-yl]-4-(2-oxo-4-phenyl-2,3-dihydro-1h-imidazol-1-yl)piperidine-1-carboxamideHCID 1146668065.5%

Reaction Steps

Diisopropylethylamine (0.020 mL, 0.11 mmol) and phosgene (0.06 mL, 0.56 mmol) were added to a solution of 4-(2-oxo-4-phenyl-2,3-dihydro-1H-imidazol-1-yl)piperidinium chloride (27 mg, 0.111 mmol) in dichloromethane (1 mL) at 0° C. After 30 min, the mixture was concentrated in vacuo and azeotroped with dichloromethane (2×) to give the crude amine. Diisopropylethylamine (0.04 ml, 0.22 mmol) was added to a solution of the crude amine and (3R,7R)-3-amino-1-(cyclopropylmethyl)-7-phenylazepan-2-one (28.7 mg, 0.11 mmol) in dichloromethane (1 mL) and the mixture heated to reflux. After 15 min, the mixture was concentrated and purified by silica gel chromatography (1% methanol/dichloromethane—5% methanol/dichloromethane) gave the title compound (38 mg). MS 528.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491713B2
Source datasetuspto-grants-2009_02
ORD IDord-41494fcac4b646c5975656cafba9334e
Source noteuspto-grants-2009_02