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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097597Generated: October 31, 2026

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

https://huagongshe.com/reaction/1097597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-BOC-ethylenediamineHCID 187201—
Reactant2,4-Dichloro-3-nitroquinolineHCID 2785138—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 2-[(2-chloro-3-nitroquinolin-4-yl)amino]ethylcarbamateHCID 8661688194.9%

Reaction Steps

Triethylamine (30.98 g, 306.1 mmol) was added to a solution of 2,4-dichloro-3-nitroquinoline (50.0 g, 204 mmol) in DMF (200 mL). A solution of N-Boc-ethylenediamine (32.7 g, 204 mmol) in DMF (100 mL) was then added in small portions. The reaction was stirred at room temperature, and then most of the DMF was removed under reduced pressure. Water (600 mL) was added to the residue, and the mixture was stirred for three hours. A solid formed and was isolated by filtration, washed with water, and dried under house vacuum to provide 71 g of tert-butyl 2-[(2-chloro-3-nitroquinolin-4-yl)amino]ethylcarbamate as a yellow solid. A portion of the material (15 g) was dissolved in dichloromethane (200 mL), and the resulting solution was washed with brine (2×100 mL) and deionized water (2×100 mL), dried over magnesium sulfate, filtered, concentrated under reduced pressure, and further dried on a vacuum pump for three days to provide 13.99 g of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143270B2
Source datasetuspto-grants-2012_03
ORD IDord-80caf528aa55472f8e1bfb82de3a059b
Source noteuspto-grants-2012_03