HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887455Generated: October 30, 2026
Sodium Carbonate → 2-(3,6-dihydro-2H-pyran-4-yl)-3-fluoropyrazine
https://huagongshe.com/reaction/887455
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3,6-Dihydro-2H-pyran-4-boronic acid pinacol ester | HCID 11218053 | — |
| Reactant | 2-Fluoro-3-iodopyrazine | HCID 15369693 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-(3,6-dihydro-2H-pyran-4-yl)-3-fluoropyrazine | HCID 59351178 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247418B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-ecdee94e7fcd40d88591c7dd8e7f5aa3 |
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| Source note | uspto-grants-2012_08 |
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