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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081700Generated: October 26, 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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[1-(3-nitrobenzyl)indol-5-ylcarbonyl]-2-methylbenzene sulphonamideHCID 19780401—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductN-[1-(3-aminobenzyl)indol-5-ylcarbonyl]-2-methylbenzene sulphonamideHCID 19780416—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05185361
Source datasetuspto-grants-1993_02
ORD IDord-845656225af949548418a55035863d1e
Source noteuspto-grants-1993_02