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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606063Generated: October 26, 2026

Triethylamine → Tert-butyl 2-[(2-chloro-3-nitroquinolin-4-yl)amino]ethylcarbamate

https://huagongshe.com/reaction/606063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCarbonic acid, bis(1,1-dimethylethyl) esterHCID 10219638—
ReactantN-(2-chloro-3-nitroquinolin-4-yl)ethane-1,2-diamineHCID 86247617—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 2-[(2-chloro-3-nitroquinolin-4-yl)amino]ethylcarbamateHCID 8661688190.1%

Reaction Steps

Triethylamine (3.12 mL, 22.4 mmol) was added to a slurry of N-(2-chloro-3-nitroquinolin-4-yl)ethane-1,2-diamine (3.00 g, 11.2 mmol) in dichloromethane (80 mL). A solution of di-tert-butyl carbonate (2.95 g, 13.5 mmol) in dichloromethane (20 mL) was added over 5 minutes to the slurry. The solution was stirred at room temperature for three hours and then was partitioned between dichloromethane and saturated aqueous sodium bicarbonate. The aqueous layer was extracted with dichloromethane. The organic layers were combined and washed with brine, dried over magnesium sulfate, filtered, and concentrated to an orange solid. The crude product was purified by flash chromatography (silica gel, 3:1 hexanes/ethyl acetate as the eluent) to afford tert-butyl 2-[(2-chloro-3-nitroquinolin-4-yl)amino]ethylcarbamate (3.70 g) as a bright yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915281B2
Source datasetuspto-grants-2011_03
ORD IDord-0222456098194ee8a8443a84aac4e7b4
Source noteuspto-grants-2011_03