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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241301Generated: November 1, 2026

Benzyl Chloride → Methyl 4-benzyl-3-oxo-3,4-dihydropyrazine-2-carboxylate

https://huagongshe.com/reaction/2241301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantLithium hydrideHCID 62714—
ReactantMethyl 3-hydroxypyrazine-2-carboxylateHCID 1514283—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-benzyl-3-oxo-3,4-dihydropyrazine-2-carboxylateHCID 6734856664.2%

Reaction Steps

LiH (7.8 mg, 0.980 mmol) was added to the solution of methyl 3-oxo-3,4-dihydropyrazine-2-carboxylate (100 mg, 0.65 mmol) in DMF (3 mL) at 0° C. After 30 minutes stirring, (chloromethyl)benzene (0.15 mL, 1.30 mmol) was added to the reaction mixture at 0° C., and then the reaction was warmed to room temperature. After stirring for 4 hours, the reaction mixture was quenched with ice water, extracted with EtOAc, washed with brine, dried over MgSO4, and concentrated to give the crude material that was purified by silica gel flash column chromatography (2% MeOH in CH2Cl2) to afford 0.102 g (64%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723330B2
Source datasetuspto-grants-2010_05
ORD IDord-17949065ca0f4eeca22acebe4fa0b116
Source noteuspto-grants-2010_05