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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353639Generated: October 29, 2026

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

https://huagongshe.com/reaction/353639

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 numberUS06753322B2
Source datasetuspto-grants-2004_06
ORD IDord-fd09094a1e5f459c91921fc8190f3e90
Source noteuspto-grants-2004_06