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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 10508Erstellt: 23. Oktober 2026

5-Bromoisoquinoline → N-(tert-butoxycarbonyl)-N-methyl-N'-(5-isoquinolyl)-1,3-propylenediamine

https://huagongshe.com/de/reaction/10508

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-BromoisoquinolineHCID 736487—
Edukt2-(Di-tert-butylphosphino)biphenylHCID 2734215—
Edukttert-butyl N-(3-aminopropyl)-N-methylcarbamateHCID 2756543—
EduktSodium t-butoxideHCID 23676156—
LösungsmittelTolueneHCID 1140—
ProduktN-(tert-butoxycarbonyl)-N-methyl-N'-(5-isoquinolyl)-1,3-propylenediamineHCID 2197988385,1%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

Under nitrogen atmosphere, a suspension of 5-bromoisoquinoline (252 mg), tris(dibenzylideneacetone)palladium(0) (59 mg), 2-(di-tert-butylphosphino)biphenyl (74 mg), (3-aminopropyl)methylcarbamic acid tert-butyl ester (274 mg, Asta Tech), and sodium tert-butoxide (163 mg) in toluene was stirred with heating at 70° C. for 3 hours. The reaction mixture was returned to room temperature and purified by silica gel column chromatography (n-hexane:ethyl acetate=1:1) to obtain the title compound (325 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07094789B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-34859159c1f24492b072bc7bfbc36a45
Quellennotizuspto-grants-2006_08