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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336868Generated: October 25, 2026

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

https://huagongshe.com/reaction/336868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
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 NNaOH 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 numberUS08889706B2
Source datasetuspto-grants-2014_11
ORD IDord-076b882cf409432d86bd7f4ecf398f0e
Source noteuspto-grants-2014_11