Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507659Generated: October 30, 2026

Triethylamine → HCID 86668859, compound

https://huagongshe.com/reaction/1507659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 86668860HCID 86668860—
SolventTolueneHCID 1140—
ProductHCID 86668859HCID 8666885960.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of (1R)-benzyl 3-amino-3-(2-aminoethyl)cyclopentanecarboxylate (from step D, 30 mg, 0.114 mmol) in toluene (2 mL) was added triethylamine (0.048 mL, 0.343 mmol) and 1,1′-Carbonyldiimidazole (37.1 mg, 0.229 mmol). The resulting mixture was stirred at 80° C. for 2 hours. To the reaction mixture was added ethyl acetate (10 mL) and the resulting mixture was washed with 1N hydrogen chloride (1 mL), water (2 mL), brine (2 mL), dried over Na2SO4 and concentrated under reduced pressure to yield (2R)-benzyl 7-oxo-6,8-diazaspiro[4.5]decane-2-carboxylate (20 mg, 0.069 mmol, 60.7% yield) as an oil. It was used as such for the subsequent step without further purification. MS (ESI+) m/z 288 M+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221819B2
Source datasetuspto-grants-2015_12
ORD IDord-fb8fb56c698b4ff3896507f63ba5a91e
Source noteuspto-grants-2015_12