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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612137Generated: October 30, 2026

3-Bromoaniline → HCID 11144112, compound

https://huagongshe.com/reaction/612137

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromoanilineHCID 11562—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Chloro-7-ethoxy-6-nitroquinoline-3-carbonitrileHCID 11011305—
SolventEthanolHCID 702—
ProductHCID 11144112HCID 1114411282.8%

Reaction Steps

A mixture of 2.1 g (7.6 mmol) of 4-chloro-7-ethoxy-6-nitro-3-quinolinecarbonitrile and 0.91 ml (8.3 mmol) of 3-bromo aniline in 100 ml ethanol was refluxed under nitrogen for 4.5 hours. The reaction mixture was poured into diluted sodium bicarbonate solution. Ethanol was removed under vacuum. The mixture was diluted with ethyl acetate and the organic layer was separated and dried over sodium sulfate. The solution was concentrated and solid was collected and then washed with hexane. Upon drying, 2.6 g of yellow solid obtained: mass spectrum (electrospray, m/e) M+H 412.8 and 414.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06002008
Source datasetuspto-grants-1999_12
ORD IDord-f3569739a62249df9a8cf57e85be3ae8
Source noteuspto-grants-1999_12