HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 508128Erstellt: 25. Oktober 2026
m-Chloroperbenzoic acid → 4-[5-(3,5-dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N-[2-(methylsulfinyl)ethyl]-1-naphthalenecarboxamide
https://huagongshe.com/reaction/508128
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | m-Chloroperbenzoic acid | HCID 70297 | — |
| Edukt | 4-[5-(3,5-dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N-[2-(methylthio)ethyl]-1-naphthalenecarboxamide | HCID 68515361 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-[5-(3,5-dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N-[2-(methylsulfinyl)ethyl]-1-naphthalenecarboxamide | HCID 68512816 | 99% |
Reaktionsschritte
To a stirred solution of 4-[5-(3,5-dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N-[2-(methylthio)ethyl]-1-naphthalenecarboxamide (i.e. the title product of Step A) (100 mg) in dichloromethane (10 mL) was added MCPBA (47 mg, 70%) at −78° C. The reaction mixture was stirred at −78 to −70° C. for 2.5 h, then quenched with saturated sodium bicarbonate, extracted with dichloromethane, washed with brine, dried with sodium sulfate, and concentrated to afford the title compound as a white solid (102 mg, 99% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09095138B2 |
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| Quelldatensatz | uspto-grants-2015_08 |
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| ORD ID | ord-49fa83d51c164048ac5a80e92b46dc1b |
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| Quellennotiz | uspto-grants-2015_08 |
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