Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409861Generated: October 25, 2026

2-nitro-5-(piperidin-1-yl)-N-(1-(3-(trifluoromethyl)phenyl)-1H-imidazol-4-yl)benzamide → 2-amino-5-(piperidin-1-yl)-N-(1-(3-(trifluoromethyl)phenyl)-1H-imidazol-4-yl)benzamide

https://huagongshe.com/reaction/2409861

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-nitro-5-(piperidin-1-yl)-N-(1-(3-(trifluoromethyl)phenyl)-1H-imidazol-4-yl)benzamideHCID 68069774—
CatalystPalladiumHCID 23938—
SolventDichloromethane methanolHCID 21226129—
Product2-amino-5-(piperidin-1-yl)-N-(1-(3-(trifluoromethyl)phenyl)-1H-imidazol-4-yl)benzamideHCID 6658741194.4%

Reaction Steps

Into a 100-mL round-bottom flask, was placed a solution of 2-nitro-5-(piperidin-1-yl)-N-(1-(3-(trifluoromethyl)phenyl)-1H-imidazol-4-yl)benzamide (600 mg, 1.11 mmol, 1.00 equiv, 85%) in methanol/dichloromethane (10/5 mL). The mixture was treated with Pd/C (600 mg) and stirred under an atmosphere of hydrogen overnight at room temperature. The solids were filtered out. The resulting mixture was concentrated under vacuum to give 450 mg (85%) of product as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815910B2
Source datasetuspto-grants-2014_08
ORD IDord-b28d5489fa0945be8c46d94d4dcd7c82
Source noteuspto-grants-2014_08