HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1509840Erstellt: 24. Oktober 2026
Niclosamide → 4-Chloro-2-(2-chloro-4-nitrophenylcarbamoyl)phenyl benzoate
https://huagongshe.com/de/reaction/1509840
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Niclosamide | HCID 4477 | — |
| Edukt | Benzoyl chloride | HCID 7412 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | 4-Chloro-2-(2-chloro-4-nitrophenylcarbamoyl)phenyl benzoate | HCID 23966630 | — |
Reaktionsschritte
A suspension of 5-Chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide (1.27 g., 3.88 mmol) in pyridine (15 mL) was treated with 4-dimethylaminopyridine (30 mg) and benzoyl chloride (0.49 mL, 4.27 mmol) was introduced dropwise. The suspension was warmed to 50° C. for one hour then cooled to room temperature and stirred for 17 hours. The reaction mixture was partitioned between 1N aqueous HCl and ethyl acetate. The ethyl acetate phase was washed with water, then brine, dried over magnesium sulfate, and concentrated to an off-white solid. This was recrystallized from ethyl acetate/hexanes. 1HNMR (500 MHz, DMSO-d6): δ7.70 (M, 3H), 7.73 (m, 2H), 7.89 (m, 1H), 7.93 (M, 1H), 8.19 (m, 1H), 8.32 (m, 1H), 10.60 (s, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08211882B2 |
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| Quelldatensatz | uspto-grants-2012_07 |
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| ORD ID | ord-c46173826d29412897e87d842c4660f2 |
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| Quellennotiz | uspto-grants-2012_07 |
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