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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359137Generated: October 31, 2026

1-benzoyl-5-nitro-1H-indole → HCID 9856121, compound

https://huagongshe.com/reaction/1359137

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-benzoyl-5-nitro-1H-indoleHCID 9835071—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventPalladiumHCID 23938—
SolventAmmonium formateHCID 2723923—
ProductHCID 9856121HCID 985612156%

Reaction Conditions

Temperature30 °C

Reaction Steps

1-benzoyl-5-nitro-1H-indole (50 mg) was dissolved in a mixed solvent with methanol (2 ml) and tetrahydrofuran (2 ml), and ammonium formate of an excess amount and palladium/carbon (10%) of a catalytic amount were added. The reacted solution was stirred at around 30° C. for 30 minutes to complete the reduction, filtered through celite and then, concentrated under reduced pressure. Afterward, the residue was dissolved again in ethylacetate (10 ml), washed with water and brine, dried over anhydrous magnesium sulfate, concentrated under reduced pressure and then, triturated with isooctane and isopropyleter. As a result, the present compound (25 mg, productive yield 56%) was obtained as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599929B2
Source datasetuspto-grants-2003_07
ORD IDord-419943ebf2e0475d976431e20c35e3fa
Source noteuspto-grants-2003_07