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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606033Generated: October 26, 2026

Potassium Carbonate → N4-allyl-2-chloroquinoline-3,4-diamine

https://huagongshe.com/reaction/606033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium dithionateHCID 146045—
ReactantN-allyl-2-chloro-3-nitroquinolin-4-amineHCID 59007293—
Catalyst1,1'-Diethyl-4,4'-bipyridinium dibromideHCID 11474262—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN4-allyl-2-chloroquinoline-3,4-diamineHCID 5900730464.6%

Reaction Steps

An aqueous solution (200 mL) of potassium carbonate (55.3 g, 400 mmol) and sodium dithionate (62.7 g, 360 mmol) was added dropwise over 30 minutes to a mixture of N-allyl-2-chloro-3-nitroquinolin-4-amine (21.0 g, 79.9 mmol) and ethyl viologen dibromide (1.80 g, 4.80 mmol) in dichloromethane (320 mL) and water (40 mL) under a nitrogen atmosphere. The dark blue-green mixture was stirred rapidly and was heated at reflux overnight. The mixture was transferred to a separatory funnel and the layers were separated. The aqueous layer was extracted with dichloromethane. The combined organic layers were filtered through CELITE filter agent, dried over magnesium sulfate, filtered, and concentrated to a dark oil. The crude product was purified by suction filter chromatography (silica gel, gradient elution from 3:1 to 1:3 hexanes/ethyl acetate, then 4:1 dichloromethane/ethyl acetate) to afford pure product N4-allyl-2-chloroquinoline-3,4-diamine (12.06 g) along with some impure product (3.10 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915281B2
Source datasetuspto-grants-2011_03
ORD IDord-ad46a58806bb476ab51f9ae1f5a3a121
Source noteuspto-grants-2011_03