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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15872Erstellt: 24. Oktober 2026

Diisopropylethylamine → N-(3-{2-[4-(2-methyl-5-quinazolinyl)-1-piperazinyl]ethyl}phenyl)methanesulfonamide

https://huagongshe.com/de/reaction/15872

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktHCID 57444358HCID 57444358—
Edukt2-{3-[(Methylsulfonyl)amino]phenyl}ethyl methanesulfonateHCID 57444359—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-(3-{2-[4-(2-methyl-5-quinazolinyl)-1-piperazinyl]ethyl}phenyl)methanesulfonamideHCID 5744435737,6%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 2-methyl-5-(1-piperazinyl)quinazoline (50 mg), 2-{3-[(methylsulfonyl)amino]phenyl}ethyl methanesulfonate (65 mg), diisopropylethylamine (192 μL) and DMF (0.5 mL) was heated to 100° C. in a sealed tube and stirred for 24 hours. The mixture was cooled to room temperature and partitioned between aqueous ammonium chloride solution and ethyl acetate. The organic layer was washed (water, brine), dried (sodium sulfate) and concentrated in vacuo. The residue was purified by column chromatography [SiO2; DCM-MeOH: (100:0)→(95:5)] to give the title compound as a beige foam (35 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732600B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-54de705710c246bd894c0bfe20ad94e2
Quellennotizuspto-grants-2010_06