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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9417Generated: October 26, 2026

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

https://huagongshe.com/reaction/9417

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 numberUS07091214B2
Source datasetuspto-grants-2006_08
ORD IDord-440122c60b11499ca2604e0ffa81145b
Source noteuspto-grants-2006_08