HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73233Generated: October 28, 2026
Hydrochloric Acid → N-(5-tert-butyl-isoxazol-3-yl)-2-methyl-2-(propane-1-sulfonyl)-propionamide
https://huagongshe.com/reaction/73233
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Sodium propane-1-sulfinate | HCID 23706191 | — |
| Reactant | 2-bromo-N-(5-tert-butyl-isoxazol-3-yl)-2-methyl-propionamide | HCID 59662626 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(5-tert-butyl-isoxazol-3-yl)-2-methyl-2-(propane-1-sulfonyl)-propionamide | HCID 25007626 | 49.4% |
Reaction Steps
To a solution of 160 mg (0.55 mmol) of 2-bromo-N-(5-tert-butyl-isoxazol-3-yl)-2-methyl-propionamide in DMF (3 mL) were added 87 mg (0.71 mmol) of 1-propanesulfinic acid sodium salt in one portion. Pyridine (48 μL) was added and the reaction was stirred at 50° C. for 18 h. The mixture was acidified with 1M aqueous HCl solution (1 mL) and extracted with diethyl ether (3×3 mL). The combined organic layers were dried over Na2SO4 and filtered. The filtrate was concentrated under reduced pressure. The crude material was purified by column chromatography (silica, eluent heptanes, 0-20% ethyl acetate) to afford 86 mg of N-(5-tert-butyl-isoxazol-3-yl)-2-methyl-2-(propane-1-sulfonyl)-propionamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829034B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-918a5ad2fd544929b63b2390f2ebc861 |
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| Source note | uspto-grants-2014_09 |
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