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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387222Generated: November 1, 2026

Ethyl Acetate → (3-Amino-5-methyl-pyrazin-2-yl)-phenyl-methanone

https://huagongshe.com/reaction/2387222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Amino-5-methyl-pyrazin-2-carboxylic acid methoxy-methyl-amideHCID 86669772—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
Product(3-Amino-5-methyl-pyrazin-2-yl)-phenyl-methanoneHCID 68631897—

Reaction Conditions

Temperature-78 °C

Reaction Steps

3-Amino-5-methyl-pyrazin-2-carboylic acid methoxy-methyl-amide (0.3 g, 1.53 mmol) is dissolved in anhydrous THF (30 ml) under N2. The clear yellow solution is cooled to −78° C., and a 1M solution of phenyl magnesium bromide in THF (7.6 ml, 7.6 mmol) is added. The resulting reaction mixture is stirred at −78° C. for 1 hour, and is then allowed to warm to room temperature and stirred for a further 2.5 hours. The reaction mixture is poured onto aq. NaHCO3 and EtOAc. The phases are separated and the aqueous layer is washed with EtOAc. The combined organic layers are washed with brine, dried (MgSO4) and concentrated in vacuo. Purification by flash chromatography (SiO2, 0-7% MeOH in DCM) yields (3-amino-5-methyl-pyrazin-2-yl)-phenyl-methanone as a yellow solid. [M+H]+ 214.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268834B2
Source datasetuspto-grants-2012_09
ORD IDord-218faaeca2ef45c4b9c74c61bd0ccd10
Source noteuspto-grants-2012_09