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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555868Generated: November 3, 2026

Sodium Carbonate → 2-(3,6-dihydro-2H-pyran-4-yl)-3-fluoropyrazine

https://huagongshe.com/reaction/555868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3,6-Dihydro-2H-pyran-4-boronic acid pinacol esterHCID 11218053—
Reactant2-Fluoro-3-iodopyrazineHCID 15369693—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(3,6-dihydro-2H-pyran-4-yl)-3-fluoropyrazineHCID 59351178—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a glass microwave vial was added 2-fluoro-3-iodopyrazine (1.6485 g, 7.36 mmol), 2-(3,6-dihydro-2H-pyran-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (2.319 g, 11.04 mmol), trans-dichlorobis(triphenylphosphine) palladium (II) (0.413 g, 0.589 mmol), and sodium carbonate (3.90 g, 36.8 mmol) in DME (19.63 mL) and water (4.91 mL) to stir at 80° C. overnight. Reaction was allowed to cool to room temperature. The reaction mixture was diluted with water and extracted with DCM. The organic extract was washed with water, brine, dried with magnesium sulfate, filtered, and concentrated. The crude product was adsorbed onto a plug of silica gel and chromatographed through a Biotage pre-packed silica gel column (40S), eluting with a gradient of 10% to 100% EtOAc in hexane, to provide 2-(3,6-dihydro-2H-pyran-4-yl)-3-fluoropyrazine. [M+H]=181.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053438B2
Source datasetuspto-grants-2011_11
ORD IDord-59d79e86475d4b58aa635fe45946eaeb
Source noteuspto-grants-2011_11