HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410316Generated: October 27, 2026
Sodium Carbonate → 3-(3,6-dihydro-2H-thiopyran-4-yl)-2-fluoropyridine
https://huagongshe.com/reaction/410316
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Fluoropyridine-3-boronic acid | HCID 2783270 | — |
| Reactant | 3,6-Dihydro-2H-thiopyran-4-yl trifluoromethanesulfonate | HCID 22625751 | — |
| Catalyst | HCID 178424406 | HCID 178424406 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| Product | 3-(3,6-dihydro-2H-thiopyran-4-yl)-2-fluoropyridine | HCID 59327102 | — |
Reaction Steps
A mixture of 3,6-dihydro-2H-thiopyran-4-yl trifluoromethanesulfonate (4.0 g, 16.11 mmol), 2-fluoropyridin-3-ylboronic acid (2.498 g, 17.72 mmol), sodium carbonate (5.12 g, 48.3 mmol), and dichlorobis(tri-o-tolylphosphine)palladium(ii) (0.633 g, 0.806 mmol) in p-dioxane/H2O (10:1, 22 mL) was heated at 135° C. in 30 min. by microwave. The reaction mixture was cooled, diluted with H2O, extracted with EtOAc (3×), dried over MgSO4, concentrated and purified by ISCO (0-40% EtOAc/Hexanes) to give the expected product was a light brown oil. MS (M+1): 196.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759532B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-87013de6c6b54685b43ee908202d6f44 |
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| Source note | uspto-grants-2014_06 |
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