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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253699Generated: October 30, 2026

N-(5-nitropyrimidin-2-yl)acetamide → N-(5-aminopyrimidin-2-yl)acetamide

https://huagongshe.com/reaction/253699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(5-nitropyrimidin-2-yl)acetamideHCID 45071770—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN-(5-aminopyrimidin-2-yl)acetamideHCID 20387481—

Reaction Steps

To N-(5-nitropyrimidin-2-yl)acetamide (0.54 g, 3.0 mmol) suspended in EtOH (20 mL) under N2 was added palladium, 10 wt. % on activated carbon (0.32 g, 0.3 mmol). The reaction mixture was hydrogenated under 1 atm of H2 at RT for 2 h and then filtered through a pad of celite and washed with MeOH. The filtrate was concentrated to give N-(5-aminopyrimidin-2-yl)acetamide as a light-yellow solid. MS (ESI, pos. ion) m/z: 153 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872128B2
Source datasetuspto-grants-2011_01
ORD IDord-fd1f2a3caa724de3b8536cf547ac63e8
Source noteuspto-grants-2011_01