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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935174Generated: November 3, 2026

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

https://huagongshe.com/reaction/1935174

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

6-Amino-4-(3,4-dibromophenylamino)quinoline-3-carbonitrile (0.750 g. 1.79 mmol) in 10 mL of THF was treated with 0.217 g (2.15 mmol) of Et3N and 0.195 g (2.15 mmol) of acryloyl chloride at 0° C. under N2. After stirring overnight at 25° C., the solvent was evaporated and the residue was slurried with water and collected. The residue was boiled twice with EtOAc and then dried in vacuo (50° C.) to give 0.609 g of N-[3-cyano-4-(3,4-dibromophenylamino)quinolin-6-yl]acrylamide as a brown solid: mass spectrum (electrospray, m/e): 470.9, 472.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384051B1
Source datasetuspto-grants-2002_05
ORD IDord-eb07436af05740a1b52b7333d9cf7a9a
Source noteuspto-grants-2002_05