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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 880683Erstellt: 24. Oktober 2026

Potassium tert-butoxide → N-[2-chloro-4-(7-fluoro-3,4-dihydro-1H-isoquinolin-2-yl)-6-methylphenyl]-3,3-dimethylbutanamide

https://huagongshe.com/de/reaction/880683

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium tert-butoxideHCID 23665647—
Edukt7-Fluoro-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 45073971—
EduktN-(4-bromo-2-chloro-6-methylphenyl)-3,3-dimethylbutanamideHCID 58097339—
LösungsmittelTolueneHCID 1140—
ProduktN-[2-chloro-4-(7-fluoro-3,4-dihydro-1H-isoquinolin-2-yl)-6-methylphenyl]-3,3-dimethylbutanamideHCID 24937204—

Reaktionsschritte

Bis(dibenzylidineacetone)palladium (2 mg, 0.0035 mmol) and (2′-dicyclohexyl phosphanyl-biphenyl-2-yl)-dimethylamine (3.3 mg, 0.0084 mmol) were added to dry toluene (10 mL purged with argon) and stirred for 15 minutes under argon. Potassium tert-butoxide (197 mg, 1.75 mmol), 7-fluoro-1,2,3,4-tetrahydroisoquinoline hydrochloride salt (121 mg, 0.65 mmol) and N-(4-bromo-2-chloro-6-methylphenyl)-3,3-dimethylbutanamide (200 mg, 0.63 mmol) were then added and the reaction mixture was stirred at 90° C. overnight. The reaction mixture was then cooled to room temperature, concentrated, and purified by thin layer chromatography (dichloromethane:methanol 5%) to afford the title compound as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08993593B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-24dfc12e962a4a88872b25821479115a
Quellennotizuspto-grants-2015_03