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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415474Generated: October 28, 2026

Water → Tert-butyl 3-{[(2-chloro-3-nitroquinolin-4-yl)amino]methyl}benzylcarbamate

https://huagongshe.com/reaction/415474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactanttert-butyl N-((3-(aminomethyl)phenyl)methyl)carbamateHCID 2756043—
Reactant2,4-Dichloro-3-nitroquinolineHCID 2785138—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 3-{[(2-chloro-3-nitroquinolin-4-yl)amino]methyl}benzylcarbamateHCID 86633722115.2%

Reaction Steps

Triethylamine (12.5 mL, 0.0889 mol) and 1-(N-Boc-aminomethyl)-3-(aminomethyl)benzene (17.71 g, 74.94 mmol) were sequentially added to a solution of 2,4-dichloro-3-nitroquinoline (18.2 g, 0.0750 mol) in DMF (90 mL), and the reaction was stirred at room temperature under nitrogen for 1.5 hours. The reaction was poured into water (2 L), and the suspension was stirred for 15 minutes. Most of the water was decanted away from the resulting precipitate, which was dissolved in ethyl acetate (600 mL). The ethyl acetate was separated from a small amount of remaining water and then removed under reduced pressure. The resulting solid was dried under vacuum to provide 38.24 g of tert-butyl 3-{[(2-chloro-3-nitroquinolin-4-yl)amino]methyl}benzylcarbamate as a sticky, amber solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088790B2
Source datasetuspto-grants-2012_01
ORD IDord-a29fa9796cda4623928c8ddbffcd198f
Source noteuspto-grants-2012_01