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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767722Generated: October 31, 2026

N-(5-Nitro-pyrimidin-2-yl)-benzamide → N-(5-aminopyrimidin-2-yl)benzamide

https://huagongshe.com/reaction/1767722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(5-Nitro-pyrimidin-2-yl)-benzamideHCID 57699955—
CatalystPlatinumHCID 23939—
SolventEthanolHCID 702—
ProductN-(5-aminopyrimidin-2-yl)benzamideHCID 1149948214.2%

Reaction Steps

10% Platinum on carbon (71 mg, 0.036 mmol) was added to a solution 2-(N-benzoyl)amino-5-nitropyrimidine (733 mg, 3.00 mmol) in ethanol (100 ml) at ambient temperature and the reaction stirred for 1 hour under an atmosphere of hydrogen. The reaction was filtered through a pad of celite and the solvents were evaporated in vacuo. Purification by flash chromatography on silica gel, eluting with 5% methanol in dichloromethane yielded 2-(N-benzoyl)amino-5-aminopyrimidine (91 mg, 14% yield) as white solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235559B1
Source datasetuspto-grants-2007_06
ORD IDord-6c3114e433d3424f97430d256d64ca11
Source noteuspto-grants-2007_06