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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81492Generated: October 30, 2026

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

https://huagongshe.com/reaction/81492

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-carboxylic 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 numberUS08846687B2
Source datasetuspto-grants-2014_09
ORD IDord-c0cee2b414df4119be2a4179c79e7188
Source noteuspto-grants-2014_09