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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837008Generated: November 1, 2026

Triethylamine → tert-Butyl 2-(3-nitroquinolin-4-ylamino)ethylcarbamate

https://huagongshe.com/reaction/1837008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-BOC-ethylenediamineHCID 187201—
Reactant4-Chloro-3-nitroquinolineHCID 11275808—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 2-(3-nitroquinolin-4-ylamino)ethylcarbamateHCID 1201682392.1%

Reaction Steps

Triethylamine (66.8 g, 0.33 mol) was added to a solution of tert-butyl N-(2-aminoethyl)carbamate (55.0 g, 0.34 mol) in anhydrous dichloromethane (500 mL). 4-Chloro-3-nitroquinoline (68.2 g, 0.33 mol) was slowly added and the reaction exothermed. The reaction mixture was allowed to stir at ambient temperature overnight. The resulting precipitate was isolated by filtration to provide product as a yellow solid. The filtrate was washed with water, dried over magnesium sulfate and then concentrated under vacuum. The resulting residue was slurried with hexane and filtered to provide additional product as a yellow solid. The two crops were combined to provide 101 g of tert-butyl N-[2-(3-nitroquinolin-4-yl)aminoethyl]carbamate as a yellow solid, m.p. 157-158.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06780873B2
Source datasetuspto-grants-2004_08
ORD IDord-729e8e1ee2cb47a889d92e63a86c600a
Source noteuspto-grants-2004_08