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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361233Generated: October 30, 2026

Ammonia hydroxide → HCID 59278496, compound

https://huagongshe.com/reaction/1361233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonia hydroxideHCID 21862953—
ReactantHCID 59278335HCID 59278335—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
ProductHCID 59278496HCID 59278496—

Reaction Steps

A solution of N-(5-cyano-pyrimidin-2-yl)-N-methyl-acetamide (0.08 g, 0.45 mmol) in MeOH and 28% aqueous ammonia hydroxide (0.80 mL, 0.45 mmol) was hydrogenated over Raney-Ni catalyst using a continuous flow hydrogenation apparatus (conditions: flow rate 1 mL/minute, 25° C., 10 bar). After 2 hours, the solvent was concentrated in vacuo. The residue was purified by silica gel chromatography eluting with 5% MeOH in CH2Cl2. The major fractions were combined and the solvent was concentrated in vacuo to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879873B2
Source datasetuspto-grants-2011_02
ORD IDord-36ca984828e34936a4febc747b1ac8a8
Source noteuspto-grants-2011_02