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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1387078Erstellt: 25. Oktober 2026

Water → 3-Bromo-4-[2-(1-pyrrolidinyl)ethoxy]phenyl 6-Methoxy-2-[4-[2-(1-pyrrolidinyl)ethoxy]phenyl]benzo[b]thiophen-3-yl Ketone

https://huagongshe.com/reaction/1387078

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium hydrideHCID 24758—
Edukt1-PyrrolidineethanolHCID 76288—
Edukt3-Bromo-4-fluorophenyl 6-methoxy-2-[4-[2-(1-pyrrolidinyl)ethoxy]phenyl]benzo[b]thiophen-3-yl ketoneHCID 21182986—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-Bromo-4-[2-(1-pyrrolidinyl)ethoxy]phenyl 6-Methoxy-2-[4-[2-(1-pyrrolidinyl)ethoxy]phenyl]benzo[b]thiophen-3-yl KetoneHCID 2118262410%

Reaktionsschritte

Sodium hydride (95 mg of a 60% suspension in mineral oil; 2.4 mmol) was suspended in 22 mL of DMF in a flame-dried, argon-filled flask and stirred for about 5 min. 1-(2-Hydroxyethyl)pyrrolidine (0.23 mL; 2.0 mmol) was added and the mixture was stirred for 15 min. 3-Bromo-4-fluorophenyl 6-methoxy-2-[4-[2-(1-pyrrolidinyl)ethoxy]phenyl]benzo[b]thiophen-3-yl ketone in 3 mL of DMF was then added. The mixture was stirred for 4 h at room temperature, then poured into water (25 mL), and extracted with EtOAc (4×25 mL). The combined organics were washed with brine and dried over magnesium sulfate. The title compound (135 mg; 10% yield) was isolated by flash chromatography on silica gel eluting with a gradient of EtOAc(100-90%)/Et3N(0-5%)/MeOH(0-5%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06265575B1
Quelldatensatzuspto-grants-2001_07
ORD IDord-15e3448c1f214af6a0bb736324e139de
Quellennotizuspto-grants-2001_07