HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884903Generated: October 31, 2026
Methanol → 6-Chloro-2-(3-methoxypyridin-4-yl)-5-(trifluoromethyl)benzoxazole
https://huagongshe.com/reaction/884903
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Chloro-2-(3-fluoropyridin-4-yl)-5-(trifluoromethyl)benzoxazole | HCID 66880110 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Chloro-2-(3-methoxypyridin-4-yl)-5-(trifluoromethyl)benzoxazole | HCID 66880558 | 44.7% |
Reaction Steps
A mixture of 0.28 g of 6-chloro-2-(3-fluoropyridin-4-yl)-5-(trifluoromethyl)benzoxazole, 0.24 g of potassium carbonate and 3 ml of methanol was stirred while heating at 60° C. for two hours. Water was added to the reaction mixture, followed by extraction with ethyl acetate twice. The combined organic layers were washed with a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 0.13 g of 6-chloro-2-(3-methoxypyridin-4-yl)-5-(trifluoromethyl)benzoxazole (hereinafter, referred to as “active compound 91”).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242133B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-787c4d2d3e204d7595b661d9c96421a0 |
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| Source note | uspto-grants-2012_08 |
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