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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934964Generated: October 31, 2026

3-Bromoaniline → HCID 5328873, compound

https://huagongshe.com/reaction/1934964

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromoanilineHCID 11562—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 10539447HCID 10539447—
SolventEthanolHCID 702—
ProductHCID 5328873HCID 532887386.1%

Reaction Steps

A mixture of 1.00 g (3.82 mmol) of 4-chloro-6-ethoxy-7-methoxyquinoline-3-carbonitrile and 0.788 g (4.58 mmol) of 3-bromoaniline in 20 mL of ethanol was refluxed under N2 for 7 h. Saturated NaHCO3 was added, volatile material was removed and the residue was azeotroped with ethanol. The crude product was slurried with hexane, filtered, washed with water and dried. Recrystallization from ethanol gave 1.31 g of 4-(3-bromophenylamino)-6-ethoxy-7-methoxyquinoline-3-carbonitrile as tan crystals: mass spectrum (electrospray, m/e): M+H 397.9, 399.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384051B1
Source datasetuspto-grants-2002_05
ORD IDord-1737213ee9244b11b258575292a94f3f
Source noteuspto-grants-2002_05