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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818167Generated: October 26, 2026

Sodium Dithionite → 7-bromo-N4-(4-chlorobutyl)quinoline-3,4-diamine

https://huagongshe.com/reaction/1818167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium DithioniteHCID 24489—
Reactant(7-Bromo-3-nitroquinolin-4-yl)-(4-chlorobutyl)amineHCID 21984395—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product7-bromo-N4-(4-chlorobutyl)quinoline-3,4-diamineHCID 6881792998%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of (7-bromo-3-nitroquinolin-4-yl)-(4-chlorobutyl)amine (8.05 g, 22.5 mmol) in methanol (250 mL) was cooled to 0° C.; a solution of sodium hydrosulfite (19.5 g, 112 mmol) in water (80 mL) was added dropwise over a period of 30 minutes. The reaction was stirred at ambient temperature for two hours and then concentrated under reduced pressure. The residue was partitioned between dichloromethane (300 mL) and aqueous sodium bicarbonate (150 mL of 50%). The aqueous layer was separated and extracted with dichloromethane (2×50 mL). The combined organic fractions were dried over magnesium sulfate, filtered, and concentrated under reduced pressure to provide 7.25 g of crude 7-bromo-N4-(4-chlorobutyl)quinoline-3,4-diamine as a light brown semi-solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598382B2
Source datasetuspto-grants-2009_10
ORD IDord-1dc53950bbaf4b52be18f80b3c89ab8a
Source noteuspto-grants-2009_10