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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 496741Erstellt: 24. Oktober 2026

N,N-bis(3-aminopropyl)methylamine → 6-(3-{methyl-[3-(7-oxo-7H-5,9-diaza-benzo[c]fluoren-6-ylamino)-propyl]-amino}-propylamino)-5,9-diaza-benzo[c]fluoren-7-one

https://huagongshe.com/de/reaction/496741

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N-bis(3-aminopropyl)methylamineHCID 7777—
EduktPotassium CarbonateHCID 11430—
EduktHCID 20829786HCID 20829786—
LösungsmittelDichloromethaneHCID 6344—
Produkt6-(3-{methyl-[3-(7-oxo-7H-5,9-diaza-benzo[c]fluoren-6-ylamino)-propyl]-amino}-propylamino)-5,9-diaza-benzo[c]fluoren-7-oneHCID 10393889—

Reaktionsschritte

A mixture of toluene-4-sulfonic acid 7-oxo-7H-5,9-diaza-benzo[c]fluoren-6-yl ester (Reference Example 6c-2) (90 mg) and N1-(3-amino-propyl)-N1-methyl-propane-1,3-diamine (WAKO PURE CHEMICAL: 15 mg) and potassium carbonate (37 mg) was suspended in dichloromethane (10 ml) and heated at reflux temperature for five days under nitrogen. The mixture was roughly purified by short silica gel column chromatography developed by dichloromethane-methanol=100:1 and dichloromethane-methanol=1:1. The fractions that contained the desired product were combined and evaporated to dryness and purified again by silica gel thin layer chromatography developed by dichloromethane-methanol-ammonia water=90:10:1. The desired compound was obtained as a dark reddish powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06946472B2
Quelldatensatzuspto-grants-2005_09
ORD IDord-47ebe698c6114793aab8c2c5be8b4eb9
Quellennotizuspto-grants-2005_09