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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499566Generated: November 1, 2026

Hydrochloric Acid → 3-Amino-6-(2,6-difluorophenyl)-2-pyrazinecarboxylic acid

https://huagongshe.com/reaction/1499566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantHCID 86726788HCID 86726788—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-Amino-6-(2,6-difluorophenyl)-2-pyrazinecarboxylic acidHCID 8672678969.6%

Reaction Steps

A solution of methyl 3-amino-6-(2,6-difluorophenyl)pyrazine-2-carboxylate (258 mg, 0.973 mmol) and lithium hydroxide monohydrate (200 mg, 4.8 mmol) in THF (4.0 mL) and water (2.0 mL) was heated at 60° C. in a sealed vial for 2 h. The reaction mixture was allowed to cool to ambient temperature and neutralized by the addition of 1.0 M hydrogen chloride in water (4.8 mL, 4.8 mmol) to form a precipitate. The precipitate was collected by filtration, washed with EtOAc (5 mL), and dried under vacuum to afford the sub-title compound (170 mg). The filtrate was diluted with EtOAc (15 mL) and the layers were separated. The organic layer was washed with H2O (3 mL) and the combined aqueous phases were extracted with EtOAc (3 mL). The combined organic layers were washed with brine (3 mL), dried over Na2SO4, filtered and concentrated under reduced pressure to provide additional sub-title compound. The crude product was used in the subsequent reaction without further purification (70 mg). LC/MS (ESI) calc. for C11H8F2N3O2(M+H)+: m/z=252.1. found: 251.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200004B2
Source datasetuspto-grants-2015_12
ORD IDord-b63ad10d44dd492bb6bfe45d95cb3cad
Source noteuspto-grants-2015_12