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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627689Generated: October 30, 2026

Dimethylformamide → Methyl 6-chloro-3-methylpyrazine-2-carboxylate

https://huagongshe.com/reaction/627689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantMethyl 3-methyl-1-oxidopyrazin-1-ium-2-carboxylate;methyl 3-methyl-4-oxidopyrazin-4-ium-2-carboxylateHCID 86728143—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductMethyl 6-chloro-3-methylpyrazine-2-carboxylateHCID 57992035106%
ProductMethyl 5-chloro-3-methylpyrazine-2-carboxylateHCID 7221858048.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of mixture of 2-(methoxycarbonyl)-3-methylpyrazine 1-oxide compound with 3-(methoxycarbonyl)-2-methylpyrazine 1-oxide (1:1) (5.1 g, 15.17 mmol) in toluene (50 mL) was cooled to 0° C. To the mixture was added phosphorus oxychloride (2.78 ml, 30.3 mmol) under nitrogen followed by n,n′-dimethylformamide (0.117 ml, 1.517 mmol). The reaction mixture was stirred at room temperature for 4 h and then was heated to 65° C. for 18 h. The mixture was cooled to room temperature, diluted with EtOAc and washed with saturated NaHCO3 solution. The aqueous layer was back-extracted with EtOAc. The combined organic extracts were dried (MgSO4), filtered and concentrated in vacuo. The mixture was purified with ISCO (0% to 50% EtOAc/Hexanes) to afford both isomers: methyl 5-chloro-3-methylpyrazine-2-carboxylate (0.68 g, 48.1% yield) and methyl 6-chloro-3-methylpyrazine-2-carboxylate (1.5 g, 106% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309263B2
Source datasetuspto-grants-2016_04
ORD IDord-302116827bbc4f6da8e88938c8ff13c7
Source noteuspto-grants-2016_04