Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2,3-Dichloro-5-hydroxypyridine | HCID 14391672 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18459669 | HCID 18459669 | — |
Reaction Steps
At 0° C., initially 7.9 g of triethylamine and then 8.5 g of methanesulfonyl chloride were added to 11.6 g of 2,3-dichloro-5-hydroxypyridine in 150 ml of methylene chloride. The mixture was subsequently stirred at approximately 20° C. for 17 hours and then washed with 100 ml of water. The organic phase was dried over magnesium sulfate and then concentrated. The resulting crude product was purified by silica gel chromatography (mobile phase: ethyl acetate/cyclohexane (1:1)). Yield: 9.1 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06432880B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-d2f64d340e824bbeacca7ccb4f0c1dde |
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| Source note | uspto-grants-2002_08 |
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