HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504507Generated: November 1, 2026
Ammonium Chloride → HCID 117737014, compound
https://huagongshe.com/reaction/1504507
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Isoxazolamine | HCID 1810216 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 117737271 | HCID 117737271 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 117737014 | HCID 117737014 | 34.3% |
Reaction Steps
A solution of 3-aminoisoxazole (0.041 ml, 0.548 mmol) and 1-(5-bromo-4-chloro-2-methoxyphenyl)-2-oxo-1,2-dihydroquinoline-6-sulfonyl chloride (0.254 g, 0.548 mmol) in THF (5.48 ml) was cooled to 0° C., at which point LiHMDS, 1.0M in THF (1.152 ml, 1.152 mmol) was added drop wise. After 40 minutes in the ice bath, the reaction was complete and ammonium chloride (sat aq) was added and the product was extracted with ethyl acetate (×3). The combined organics were dried over magnesium sulfate, filtered and concentrated in vacuo. The crude material was purified via MPLC, eluting with 0-100% ethyl acetate in heptane to yield 1-(5-bromo-4-chloro-2-methoxyphenyl)-N-(isoxazol-3-yl)-2-oxo-1,2-dihydroquinoline-6-sulfonamide (0.096 g, 0.188 mmol, 34.3% yield) as a light-yellow solid. m/z (ESI) 510.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09212182B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-eafd449df16b44a2aeda3a8eb5a9036c |
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| Source note | uspto-grants-2015_12 |
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