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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284315Generated: November 3, 2026

HCID 67112859, compound → HCID 67113010, compound

https://huagongshe.com/reaction/2284315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67112859HCID 67112859—
ReactantHCID 178418361HCID 178418361—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
ProductHCID 67113010HCID 67113010100%

Reaction Steps

To a slurry of 1-methyl-N-(3-(4-nitrophenyl)-1H-indol-6-yl)-1H-indole-5-carboxamide (59.0 mg, 0.14 mmol) in ethanol (1.50 mL) under an atmosphere of nitrogen was added 20 wt % palladium hydroxide on carbon (5.9 mg, 10 wt %), followed by a balloon of hydrogen. The reaction was stirred overnight at room temperature and was then filtered through a pad of Celite, rinsing with excess methanol and methylene chloride. The filtrate was concentrated to give a grey-pink solid for N-(3-(4-aminophenyl)-1H-indol-6-yl)-1-methyl-1H-indole-5-carboxamide (56.9 mg, 0.14 mmol, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09144557B2
Source datasetuspto-grants-2015_09
ORD IDord-c36ccf0aa5d54ba8a7bd7d3f3a361ac4
Source noteuspto-grants-2015_09