HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 10738Erstellt: 25. Oktober 2026
4-Acetylbenzenesulphonamide → HCID 178419032, Verbindung
https://huagongshe.com/reaction/10738
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Acetylbenzenesulphonamide | HCID 74065 | — |
| Edukt | Lithium methanolate | HCID 4177230 | — |
| Edukt | HCID 178418754 | HCID 178418754 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 178419032 | HCID 178419032 | — |
Reaktionsschritte
To a solution of 4-acetyl-benzenesulfonamide (Ex-26A, 0.12 g, 0.59 mmol) and 5-(2-cyclopropyl-1H-imidazol-4-yl)-2,4-dimethoxy-benzaldehyde (Ex-105B, 0.16 g, 0.59 mmol) in N,N-dimethylformamide (16 mL) was added lithium methoxide (1.0M in methanol, 2.4 mL, 2.4 mmol). The reaction mixture was allowed to stir for 18 hours at ambient temperature. The reaction was quenched with water. The aqueous solution was extracted with dichloromethane. The combined dichloromethane was concentrated. The crude product was purified by flash chromatography. Elution with methanol (10%, v/v, in dichloromethane) gave the title compound as red solid: m.p. 156–160° C. 1H NMR (DMSO-d6) δ 11.65 (bs, 1H), 8.32 (s, 1H), 8.19 (d, J=9.0 Hz, 2H), 8.00 (d, J=15.7 Hz, 1H), 7.95 (d, J=9.0 Hz, 2H), 7.62–7.52 (m, 2H), 7.24 (bs, 1H), 6.73 (s, 1H), 3.96 (s, 3H), 3.94 (s, 3H), 1.98–1.94 (m, 1H), 0.88–0.85 (m 4H). MS m/z=454 ([M+H]+, 100%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07094801B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-bc0bededacff4f5c853c190677c0df9b |
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| Quellennotiz | uspto-grants-2006_08 |
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