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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 655911Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/655911

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
Edukt4-MethylmorpholineHCID 7972—
Edukt1-Hydroxybenzotriazole hydrateHCID 2796029—
Edukt(1S)-1-phenylpropan-1-amineHCID 6993773—
Edukt3-(Azidomethyl)-2-phenylquinoline-4-carboxylic acidHCID 57893567—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(azidomethyl)-2-phenyl-N-[(1S)-1-phenylpropyl]quinoline-4-carboxamideHCID 5789357073%

Reaktionsschritte

A solution of 3-(azidomethy)-2-phenylquinoline-4-carboxylic acid (2c) (997 mg, 3.28 mmol), HOBT hydrate (760 mg, 4.92 mmol), 4-methylmorpholine (551 μL, 4.92 mmol) in tetrahydrofuran (50 mL) was added EDC (960 mg, 4.92 mmol) at RT under N2. (S)-1-Phenyl propylamine (488.5 mg, 3.62 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 10% aqueous sodium bicarbonate solution, dried over sodium sulfate and then concentrated in vacuo. The residue was purified by chromatography eluting with 15-25% ethyl acetate/hexane to give the title compound (1000 mg, 73%) as a light-yellow solid. 1H NMR (300 MHz, CDCl3) δ 0.94 (t, 3H), 2.01 (m, 2H), 5.17 (q, 1H), 5.19 (s, 2H), 5.72 (b, 1H), 7.21 (d, 2H), 7.34 (d, 2H), 7.39 (m, 1H), 7.78 (m, 2H), 7.84 (m, 2H), 8.08 (m, 1H), 8.30 (m, 2H), 8.49 (m, 2H). MS APCI, m/z=422 (M+1). LCMS: 2.47 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08071621B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-2fb9b0e30e3141d9be927839528ba8e4
Quellennotizuspto-grants-2011_12