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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406071Generated: October 31, 2026

2-nitro-N-(2-phenylpyrimidin-5-yl)-5-(piperidin-1-yl)benzamide → 2-amino-N-(2-phenylpyrimidin-5-yl)-5-(piperidin-1-yl)benzamide

https://huagongshe.com/reaction/2406071

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-nitro-N-(2-phenylpyrimidin-5-yl)-5-(piperidin-1-yl)benzamideHCID 66586937—
CatalystPalladiumHCID 23938—
SolventEthanol ethylacetateHCID 21584252—
Product2-amino-N-(2-phenylpyrimidin-5-yl)-5-(piperidin-1-yl)benzamideHCID 6658702797%

Reaction Steps

Into a 100-mL round bottom flask, was placed a solution of 2-nitro-N-(2-phenylpyrimidin-5-yl)-5-(piperidin-1-yl)benzamide (100 mg, 0.25 mmol, 1.00 equiv) in EtOAc/EtOH (5/5 mL). The mixture was treated with Pd/C (10 mg) and stirred under a hydrogen atmosphere for 2 h at room temperature. The solids were filtered out. The resulting mixture was concentrated under vacuum to yield 90 mg (97%) of product as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809339B2
Source datasetuspto-grants-2014_08
ORD IDord-83e69760cce84ff690e82d0a5ac3c31f
Source noteuspto-grants-2014_08