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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093084Generated: November 1, 2026

Acetic Acid → Ethyl 10-(benzyl(ethyl)amino)-4-oxo-3-((phenylcarbonyl)oxy)-4,6,7,8,9,10-hexahydro-7,10-ethanopyrimido[1,2-a]azepine-2-carboxylate

https://huagongshe.com/reaction/1093084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetaldehydeHCID 177—
ReactantBenzaldehydeHCID 240—
ReactantTriethylamineHCID 8471—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantEthyl 10-amino-4-oxo-3-((phenylcarbonyl)oxy)-4,6,7,8,9,10-hexahydro-7,10-ethanopyrimido[1,2-a]azepine-2-carboxylate hydrochlorideHCID 66588778—
Solvent1,2-DichloroethaneHCID 11—
ProductEthyl 10-(benzyl(ethyl)amino)-4-oxo-3-((phenylcarbonyl)oxy)-4,6,7,8,9,10-hexahydro-7,10-ethanopyrimido[1,2-a]azepine-2-carboxylateHCID 57905266—

Reaction Steps

To a stirred solution of Ethyl 10-amino-4-oxo-3-((phenylcarbonyl)oxy)-4,6,7,8,9,10-hexahydro-7,10-ethanopyrimido[1,2-a]azepine-2-carboxylate hydrochloride (200 mg, 0.461 mmol) in 1,2-dichloroethane (10 mL) was added triethylamine (0.064 mL, 0.461 mmol) and the resulting mixture stirred for 5 min. Benzaldehyde (0.186 mL, 1.844 mmol), AcOH (0.053 mL, 0.922 mmol) and NaCNBH3 (87 mg, 1.383 mmol) were then added and the mixture stirred for 6 h. Acetaldehyde (0.182 mL, 3.23 mmol) was then added to the reaction and the this was stirred at room temperature for 16 h. The mixture was then quenched with sat. NaHCO3 and extracted with dichloromethane, dried (Na2SO4), filtered and concentrated to afford title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129398B2
Source datasetuspto-grants-2012_03
ORD IDord-cb8c9b20c93e408c93601cdf83478456
Source noteuspto-grants-2012_03