HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219287Generated: October 25, 2026
1,4-Dioxane → 2,3-Difluoro-5-(3-methylisoxazol-5-yl)pyridine
https://huagongshe.com/reaction/219287
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 3-Methyl-5-(tributylstannyl)isoxazole | HCID 2763255 | — |
| Reactant | 5-Chloro-2,3-difluoropyridine | HCID 2783248 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Product | 2,3-Difluoro-5-(3-methylisoxazol-5-yl)pyridine | HCID 58015534 | 55.4% |
Reaction Steps
A 330 mL pressure vessel was charged with 5-chloro-2,3-difluoropyridine (5.00 g, 33.4 mmol), 3-methyl-5-(tributylstannyl)isoxazole (14.9 g, 40.1 mmol), XPhos (2.23 g, 4.68 mmol), PdOAc2 (0.526 g, 2.34 mmol), and 1,4-dioxane (167 ml, 33.4 mmol), flushed with argon, sealed, then heated at 100° C. for 16 hours. The mixture was concentrated; the black oil was absorbed onto silica gel and purified by MPLC, eluting with 20% EtOAc in hexanes isocratic to yield an orange solid; this was triturated with hexanes to give 2,3-difluoro-5-(3-methylisoxazol-5-yl)pyridine (3.6278 g, 55.3% yield) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198448B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-cb12bebbeccc4a719bb91e95332a4562 |
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| Source note | uspto-grants-2012_06 |
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