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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934935Generated: November 1, 2026

Triethylamine → N-[3-cyano-4-(3,4-dibromophenylamino)quinolin-6-yl]acrylamide

https://huagongshe.com/reaction/1934935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
Reactant6-Amino-4-(3,4-dibromophenylamino)quinoline-3-carbonitrileHCID 10158966—
SolventTetrahydrofuranHCID 8028—
ProductN-[3-cyano-4-(3,4-dibromophenylamino)quinolin-6-yl]acrylamideHCID 1011620772.1%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 0.75 g (1.79 mmol) of 6-amino-4-[(3,4-dibromophenyl)amino]-3-quinolinecarbonitrile and 0.22 g (2.15 mmol) of triethylamine in 10 mL of tetrahydrofuran was added dropwise 0.195 g (2.15 mmol) of acryloyl chloride. After stirring overnight at 25° C., volatile material was removed and the residue was slurried in water and solid was collected. The crude product was washed with boiling ethyl acetate dried in vacuo (50° C.) to give 0.609 g of brown solid: high resolution mass spectrum (m/e): 470.9457.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384051B1
Source datasetuspto-grants-2002_05
ORD IDord-2cefd17b213945fd91b38a0da06cbcac
Source noteuspto-grants-2002_05