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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944591Generated: October 28, 2026

Water → Ethyl 4-(4-benzylphenylamino)-6-chloroquinoline-3-carboxylate

https://huagongshe.com/reaction/1944591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantBenzenamine, 4-(phenylmethyl)-HCID 136914—
ReactantEthyl 4,6-dichloroquinoline-3-carboxylateHCID 1479087—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 4-(4-benzylphenylamino)-6-chloroquinoline-3-carboxylateHCID 5852496571.3%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of Ethyl-4,6-dichloroquinoline-3-carboxylate (1.0 g, 3.7 mmol) in 1,4-dioxane (10 mL) was added a solution of 4-benzylbenzenamine (733 mg, 4.0 mmol) in 1,4-dioxane (10 mL) at room temperature. After stirred at 85° C. 1 hour, the reaction mixture was then cooled down to room temperature and then treated with 20 mL of water. The resulting suspension treated with 10 N NaOH solutions to reach the pH about 9. It was partitioned between ethyl acetate and water. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over MgSO4, filtered and concentrated. The crude product was purified by flash column chromatography using a 9:1 v/v hexane:ethyl acetate as solvent to afford title compound (1.1 g, 65% yield) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394818B2
Source datasetuspto-grants-2013_03
ORD IDord-e25d4976eb6a438482e1c3a4b6d729e7
Source noteuspto-grants-2013_03