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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 459711Erstellt: 24. Oktober 2026

3-Ethoxy-2-propenoyl chloride → 1,6,7,8,9,10-Hexahydro-2h-azepino[3,2-g]quinolin-2-one

https://huagongshe.com/de/reaction/459711

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Ethoxy-2-propenoyl chlorideHCID 3014429—
Edukt2,3,4,5-tetrahydro-1H-benzo[b]azepin-8-amineHCID 18444221—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelSodium HydroxideHCID 14798—
Produkt1,6,7,8,9,10-Hexahydro-2h-azepino[3,2-g]quinolin-2-oneHCID 9899244—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A solution of 2,3,4,5-tetrahydro-1H-1-benzazapin-8-amine (0.6 g, 3.4 mmol) and 3-ethoxyacryloyl chloride (0.45 g, 3.4 mmol) in CH2Cl2 (50 mL) and 3N NaOH (10 mL) was stirred for 1 h at ambient temperature. The reaction was partitioned between CH2Cl2 and water. The organic layer was concentrated and the remaining brown oil was dissolved in 70% aq. H2SO4 (20 mL) and heated gently (50° C.) for 2 h. The reaction was cooled and neutralized with aq. NH4OH and partitioned between water and EtOAc. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated. The residue was dissolved in DMF (1 mL) and purified on a GILSON automated system affixed with a YMC COMBIFLASH 50 mm×20 mm reverse phase column eluted 5–95% CH3CN in water at 30 mL/min over 10.5 min to provide pure desired product. HRMS m/z (M+1) calcd 215.1179; found 215.1186.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07196076B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-f67beddc9b33443db36a36f7388ba7e4
Quellennotizuspto-grants-2007_03