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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2081700Erstellt: 26. Oktober 2026

N-[1-(3-nitrobenzyl)indol-5-ylcarbonyl]-2-methylbenzene sulphonamide → N-[1-(3-aminobenzyl)indol-5-ylcarbonyl]-2-methylbenzene sulphonamide

https://huagongshe.com/reaction/2081700

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-[1-(3-nitrobenzyl)indol-5-ylcarbonyl]-2-methylbenzene sulphonamideHCID 19780401—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN-[1-(3-aminobenzyl)indol-5-ylcarbonyl]-2-methylbenzene sulphonamideHCID 19780416—

Reaktionsschritte

The nitrobenzylindole (Example 3) (2.7 g) was dissolved in methanol (125 ml) and ethyl acetate (125 ml), and 10% palladium on charcoal (0.5 g) added. The reaction mixture was hydrogenated in a Parr bottle at 50 p.s.i. with shaking until hydrogen uptake was complete (approximately 1 hour). The catalyst was filtered off through Celite and the solvent removed in vacuo to give N-[1-(3-aminobenzyl)indol-5-ylcarbonyl]-2-methylbenzene sulphonamide as a foam. This crude product was used in the next step without purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05185361
Quelldatensatzuspto-grants-1993_02
ORD IDord-845656225af949548418a55035863d1e
Quellennotizuspto-grants-1993_02