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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216702Generated: October 30, 2026

Ethyl 1-cyclopentyl-2-(4-nitrophenyl)benzimidazole-5-carboxylate → Ethyl 2-(4-aminophenyl)-1-cyclopentylbenzimidazole-5-carboxylate

https://huagongshe.com/reaction/2216702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 1-cyclopentyl-2-(4-nitrophenyl)benzimidazole-5-carboxylateHCID 10293086—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(4-aminophenyl)-1-cyclopentylbenzimidazole-5-carboxylateHCID 1013255299.5%

Reaction Steps

Ethyl 1-cyclopentyl-2-(4-nitrophenyl)benzimidazole-5-carboxylate (12 g) obtained in Example 21 was dissolved in tetrahydrofuran (200 ml) and ethyl alcohol (50 ml), 7.5% palladium carbon (50% wet, 1 g) was added. The mixture was hydrogenated for 1 hr at atmospheric pressure. The catalyst was filtered off and the filtrate was concentrated under reduced pressure. Tetrahydrofuran was added to the residue to allow crystallization and the crystals were collected by filtration to give the title compound (11 g, yield 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112600B1
Source datasetuspto-grants-2006_09
ORD IDord-33d3bba4662740b9bb651aef6f44ef23
Source noteuspto-grants-2006_09