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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1373610Erstellt: 26. Oktober 2026

Triethylamine → 7-{4-[4-(2,3-Dichloro-phenyl)-piperazin-1-yl]-butoxy}-5-methyl-3,4-dihydro-1H-[1,8]naphthyridin-2-one

https://huagongshe.com/reaction/1373610

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt1-(2,3-Dichlorophenyl)piperazine hydrochlorideHCID 11630372—
Edukt4-(4-Methyl-7-oxo-5,6,7,8-tetrahydro-[1,8]naphthyridin-2-yloxy)-butyraldehydeHCID 21073350—
LösungsmittelDichloromethaneHCID 6344—
Lösungsmittel1,1-DichloroethaneHCID 6365—
Produkt7-{4-[4-(2,3-Dichloro-phenyl)-piperazin-1-yl]-butoxy}-5-methyl-3,4-dihydro-1H-[1,8]naphthyridin-2-oneHCID 1156173370,5%

Reaktionsschritte

To a suspension of 1-(2,3-dichloro-phenyl)-piperazine hydrochloride (0.93 g, 3.48 mmol) in dichloroethane (10 mL) was added Et3N (0.96 mL, 6.92 mmol). The mixture was stirred for 15 min and a suspension of 4-(4-methyl-7-oxo-5,6,7,8-tetrahydro-[1,8]naphthyridin-2-yloxy)-butyraldehyde (0.86 g, 3.46 mmol) in dichloroethane (5 mL) was added. After 20 min at RT, NaBH(OAc)3 (1.03 g, 4.85 mmol) was added and the reaction was stirred at room temperature for 4 h. The reaction mixture was poured into CH2Cl2 and washed with H2O, 1N citric acid, saturated NaHCO3 and brine, dried over Na2SO4 and concentrated to an oil. Et2O was added and the organics were decanted from an insoluble gum. The filtrate yielded a crystalline solid, which was collected by filtration and dried. Purification by liquid chromatography (gradient elution, 100% CHCl3 to 2% MeOH/CHCl3, Biotage 40m column) provided the title compound as a white solid (1.12 g, 2.44 mmol, 70%). MS: APCI: M+1: 463.1 (Exact Mass: 462.16).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07160888B2
Quelldatensatzuspto-grants-2007_01
ORD IDord-f99058e8660f4b7ab497df16805c2368
Quellennotizuspto-grants-2007_01