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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902174Generated: October 30, 2026

HCID 131724381, compound → HCID 131724380, compound

https://huagongshe.com/reaction/902174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131724381HCID 131724381—
ReactantHCID 178418361HCID 178418361—
CatalystAdams' catalystHCID 345198—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131724380HCID 131724380100%

Reaction Steps

A solution of 5-nitro-3-(3,5-dimethylphenylsulfonyl)indole-2-carboxyamide (0.25 g, 0.0007 mol) in tetrahydrofuran (40 mL) and methanol (16 mL) was reduced under an atmospheric pressure of hydrogen in the presence of PtO2 (50 mg) as a catalyst for 6 hours. Catalyst was separated by filtration and the solvent evaporated to give 0.227 g (100%) of pure 5-amino-3-(3,5-dimethylphenylsulfonyl)indole-2-carboxyamide as a brown oil. A solution of the last compound (0.227 g, 0.0007 mol), 2,5-dimethoxy-tetrahydrofuran (0.09 g, 0.0006 mol) in glacial acetic acid (5 mL) was refluxed for 30 minutes. After evaporation of the solvent the residue was triturated with ice water and extracted with ethyl acetate. Organic layer was washed with brine and dried. Removal of the solvent left the crude product which was purified by passing through a silica gel column chromatography (ethyl acetate as eluent) to give 0.15 g (57%) of title compound, mp 270-272° C. (from ethanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365090B2
Source datasetuspto-grants-2008_04
ORD IDord-34116b9fa12247b7b6bbd8e2ed4bf251
Source noteuspto-grants-2008_04