Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627703Generated: November 4, 2026

Phosphorus oxychloride → Methyl 5-chloro-3-methylpyrazine-2-carboxylate

https://huagongshe.com/reaction/627703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant3-(Methoxycarbonyl)-2-methylpyrazine 1-oxideHCID 66665356—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-chloro-3-methylpyrazine-2-carboxylateHCID 7221858022%

Reaction Conditions

Temperature100 °C

Reaction Steps

In a 1-L flask, the crude 3-(methoxycarbonyl)-2-methylpyrazine 1-oxide (step 2, 17.77 g, 106 mmol) was dissolved in DMF (300 mL). Neat phosphoryl trichloride (29.6 mL, 317 mmol) was added. The reaction mixture was heated to 100° C. After 1 h, the reaction mixture was concentrated to remove most of the DMF. The flask was cooled in an ice water bath, and 1 M aqueous Na2CO3 (300 mL) was added slowly, followed by 80% EtOAc-hexane (400 mL). The mixture was filtered through Celite. The resulting filtrate was partitioned and the aqueous phase was extracted further with 80% EtOAc-hexane (2×250 mL). The combined organic layers were dried over MgSO4 and concentrated. The material was purified through silica gel using 11% EtOAc-hexane to afford the title compound (4.29 g, 23 mmol, 22%). MS m/z=187 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309263B2
Source datasetuspto-grants-2016_04
ORD IDord-5bc7e28e35b54f74a9d4b00b1742990a
Source noteuspto-grants-2016_04