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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716629Generated: October 25, 2026

3-(1H-Indol-7-yl)-N-methyl-3-phenyl-acrylamide → 3-(1H-Indol-7-yl)-N-methyl-3-phenyl-propionamide

https://huagongshe.com/reaction/1716629

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(1H-Indol-7-yl)-N-methyl-3-phenyl-acrylamideHCID 69174099—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-(1H-Indol-7-yl)-N-methyl-3-phenyl-propionamideHCID 59831745—

Reaction Steps

To a solution of 3-(1H-indol-7-yl)-N-methyl-3-phenyl-acrylamide XVIII in EtOH (8 ml) was added Degussa's catalyst (10% Pd/C wet, 55 mg). The reaction mixture was subjected to a hydrogenation reaction in a Parr apparatus at 50 psi of H2 for 20 hours. The reaction mixture was filtered through a celite pad, and the filter cake was washed with MeOH. The filtrate was concentrated affording 3-(1H-indol-7-yl)-N-methyl-3-phenyl-propionamide XIX as a white solid in quantitative yield (296 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803830B2
Source datasetuspto-grants-2010_09
ORD IDord-8247146e22e342058a653ede35b96ab0
Source noteuspto-grants-2010_09