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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10461Generated: October 28, 2026

Triethylamine → Benzyl 2-[({[2-(diisopropylamino)ethyl]amino}carbonyl)amino]ethylcarbamate

https://huagongshe.com/reaction/10461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl N-(2-aminoethyl)carbamate hydrochlorideHCID 12715871—
ReactantN-[2-(diisopropylamino)ethyl]-1H-imidazole-1-carboxamideHCID 21978296—
SolventDichloromethaneHCID 6344—
ProductBenzyl 2-[({[2-(diisopropylamino)ethyl]amino}carbonyl)amino]ethylcarbamateHCID 21978301109.6%

Reaction Steps

A solution of benzyl 2-aminoethylcarbamate hydrochloride (4.33 g, 18.8 mmol), N-[2-(diisopropylamino)ethyl]-1H-imidazole-1-carboxamide (Preparation 19) (3.73 g, 15.64 mmol) and triethylamine (2.62 ml, 18.8 mmol) in dichloromethane (100 ml) was heated under reflux for 14 hours. The solution was allowed to cool to room temperature and then washed with water (20 ml). The aqueous layer was separated and extracted with more dichloromethane (20 ml). The combined organic layers were dried over anhydrous magnesium sulfate and solvent evaporated under reduced pressure to give the title compound as a yellow oil (6.25 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094769B2
Source datasetuspto-grants-2006_08
ORD IDord-1eb4ad4101bd408cab4df1eea911d020
Source noteuspto-grants-2006_08