HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443797Generated: October 27, 2026
Water → 6-Methoxy-2-methyl-3-(5-methyl-4-isoxazolyl)pyridine
https://huagongshe.com/reaction/1443797
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Methyl-6-methoxypyridine-3-boronic acid | HCID 2763084 | — |
| Reactant | 4-Iodo-5-methylisoxazole | HCID 2795461 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 6-Methoxy-2-methyl-3-(5-methyl-4-isoxazolyl)pyridine | HCID 21071930 | 40.2% |
Reaction Steps
A mixture of 4-iodo-5-methylisoxazole (18.2 g, 87 mmol), 6-methoxy-2-methylpyridine-3-boronic acid (14.6 g, 87 mmol), sodium bicarbonate (22.0 g, 262 mmol), water (150 mL) and DME (150 mL) was degassed three times with stirring by the application of a vacuum and then introduction of a nitrogen atmosphere. [1,1-Bis(diphenylphosphino)ferrocene]-dichloropalladium (II) (2.14 g, 2.6 mmol) was added in one portion. The reaction mixture was degassed as before. The reaction mixture was then stirred at 80° C. for 4 h, then it was cooled to ambient temperature. Three extractions with EtOAc, drying the combined organic layers over MgSO4, filtration and removal of solvent in vacuo afforded an oil. Flash chromatography (EtOAc:hexane:1:9) and removal of solvent in vacuo from the desired fractions gave the product (7.15 g): 1H-NMR (CDCl3, 300 MHz): δ 8.16 (s, 1H), 7.33 (d, 1H, J=8), 6.63 (d, 1H, J=8), 3.95 (s, 3H), 2.35 (s, 64); APCI+-MS: 205 (M++14).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07662817B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-d5957487c9694a3a8d98e8d9ac606464 |
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| Source note | uspto-grants-2010_02 |
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