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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51957Generated: October 30, 2026

Morpholine → 4'-Trifluoromethyl-biphenyl-2-carboxylic acid [3-(morpholine4-carbonyl)-quinolin-7-yl]-amide

https://huagongshe.com/reaction/51957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant7-[(4'-Trifluoromethyl-biphenyl-2-carbonyl)-amino)-quinoline-3-carboxylic acidHCID 10296719—
SolventDichloromethaneHCID 6344—
Product4'-Trifluoromethyl-biphenyl-2-carboxylic acid [3-(morpholine4-carbonyl)-quinolin-7-yl]-amideHCID 1014201450.4%

Reaction Steps

7-[(4′-Trifluoromethyl-biphenyl-2-carbonyl)-amino]-quinoline-3-carboxylic acid (50 mg, 0.11 mmol) was combined with morpholine (11 mg, 0.12 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (26 mg, 0.14 mmol), 1-hydroxybenzotriazole (17 mg, 0.13 mmol), and triethylamine (0.064 ml, 0.46 mmol) in 1 ml of dichloromethane and allowed to react overnight. The reaction mixture was concentrated, the residue was suspended in water, and the solid was collected by vacuum filtration. This material was purified by preparative thin-layer-chromatography on silica eluting with ethyl acetate. The product containing band was collected and eluted with 5% methanol in ethyl acetate to afford 28 mg of the title compound as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713489B2
Source datasetuspto-grants-2004_03
ORD IDord-9b0895d510c24731838475ed2179fce3
Source noteuspto-grants-2004_03