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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2425512Erstellt: 26. Oktober 2026

1,2-Dichloroethane → 3-(ethylthio)-2-phenyl-N-[(1S)-1-phenylpropyl]quinolin-4-carboxamide

https://huagongshe.com/reaction/2425512

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
Edukt4-MethylmorpholineHCID 7972—
Edukt3-(Ethylthio)-2-phenylquinoline-4-carboxylic acidHCID 624513—
Edukt1-Hydroxybenzotriazole hydrateHCID 2796029—
Edukt(1S)-1-phenylpropan-1-amineHCID 6993773—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-(ethylthio)-2-phenyl-N-[(1S)-1-phenylpropyl]quinolin-4-carboxamideHCID 5932348785%

Reaktionsschritte

A solution of 3-(ethylthio)-2-phenylquinoline-4-carboxylic acid (4) (269 mg, 0.87 mmol), HOBT hydrate (230 mg, 1.5 mmol), 4-methylmorpholine (164 μL, 1.5 mmol) in DCM (30 ml) was added EDC (289 mg, 1.5 mmol) at RT under N2. (S)-1-Phenyl propylamine (202 mg, 1.5 mmol) was then added and the reaction mixture stirred at RT for 12 h. All solvent was removed in vacuo and the residue was partitioned between ethyl acetate and 0.5 N HCl aqueous solution. The organic phase was washed with 10% aqueous sodium bicarbonate solution, brine, and dried over sodium sulfate. The organic solution was then concentrated in vacuo. The residue was purified by chromatography eluting with 15-25% ethyl acetate/hexane to give the title compound (315 mg, 85% yield) as a solid. 1H NMR (300 MHz, CDCl3) δ 0.96 (t, 3H), 1.22 (t, 3H), 2.0 (m, 2H), 2.40 (m, 2H), 5.28 (q, 1H), 7.20 (d, 2H), 7.34 (d, 2H), 7.39 (m, 2H), 7.78 (m, 2H), 7.84 (m, 2H), 8.00 (m, 1H), 8.11 (m, 2H), 8.15 (m, 2H). MS APCI, m/z=427 (M+1). LCMS: 2.82 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07964733B2
Quelldatensatzuspto-grants-2011_06
ORD IDord-d95c1573116e4c78ac3e5899f6efa0eb
Quellennotizuspto-grants-2011_06