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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606064Generated: October 30, 2026

Sodium Dithionite → Tert-butyl 2-[(3-amino-2-chloroquinolin-4-yl)amino]ethylcarbamate

https://huagongshe.com/reaction/606064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium DithioniteHCID 24489—
ReactantTert-butyl 2-[(2-chloro-3-nitroquinolin-4-yl)amino]ethylcarbamateHCID 86616881—
SolventWaterHCID 962—
ProductTert-butyl 2-[(3-amino-2-chloroquinolin-4-yl)amino]ethylcarbamateHCID 8661688262.9%

Reaction Steps

A solution of Na2S2O4 (10.3 g, 50.4 mmol) in water (40 mL) was added to a solution of tert-butyl 2-[(2-chloro-3-nitroquinolin-4-yl)amino]ethylcarbamate (3.70 g, 10.1 mmol). A white solid precipitated immediately and after 30 min the precipitate was removed by filtration. The filtrate was concentrated under reduced pressure, was diluted with saturated aqueous sodium bicarbonate, and was extracted with dichloromethane three times. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered, and concentrated to a pale yellow oil. Purification by flash chromatography (silica gel, gradient elution with 2:1 to 1:1 hexanes/ethyl acetate) afforded tert-butyl 2-[(3-amino-2-chloroquinolin-4-yl)amino]ethylcarbamate (2.14 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915281B2
Source datasetuspto-grants-2011_03
ORD IDord-fe5cbc5da5ea4440bc6daf92dbb116ea
Source noteuspto-grants-2011_03