HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29529Erstellt: 23. Oktober 2026
p-Bromobenzenesulfonyl chloride → 4-Bromo-N-[4-chloro-2-(pyridine-4-carbonyl)-phenyl]-benzenesulfonamide
https://huagongshe.com/de/reaction/29529
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | p-Bromobenzenesulfonyl chloride | HCID 7396 | — |
| Edukt | (2-Amino-5-chlorophenyl)-pyridin-4-yl methanone | HCID 10214538 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | 4-Bromo-N-[4-chloro-2-(pyridine-4-carbonyl)-phenyl]-benzenesulfonamide | HCID 10072530 | — |
Reaktionsschritte
4-Bromo-benzenesulfonyl chloride 27.5 g (107 mmol) was dissolved in 180 ml of anhydrous pyridine. To this solution was added (2-amino-5-chloro-phenyl)-pyridin-4-yl-methanone 25 g (107 mmol). The reaction mixture was stirred under nitrogen 5 hour at 80° C. and pyridine was then evaporated under vacuum. The resulting crude material was dissolved in dichloromethane, and extracted with saturated bicarbonate solution. The combined organic layer was washed with brine dried over magnesium sulfate, filtered and concentrated, then ethyl acetate (50 mL) added to the solid, the solid was filtered, washed again with ethyl acetate, to yield a pale yellow solid: LC-MSD, m/z for C18H12BrClN2O3S [M+H]+: 452.9
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07420055B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-83614b2a73924137bac68b7eedc2daea |
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| Quellennotiz | uspto-grants-2008_09 |
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