HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1415935Erstellt: 23. Oktober 2026
Chloroform → 1-(3-Benzoylamino-4,6-difluorophenyl)-7-chloro-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid
https://huagongshe.com/de/reaction/1415935
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Chloroform | HCID 6212 | — |
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Benzoic anhydride | HCID 7167 | — |
| Edukt | 1-(3-Amino-4,6-difluorophenyl)-7-chloro-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid | HCID 11089970 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Diisopropyl Ether | HCID 7914 | — |
| Produkt | 1-(3-Benzoylamino-4,6-difluorophenyl)-7-chloro-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid | HCID 54394918 | 92,6% |
Reaktionsschritte
1-(3-amino-4,6-difluorophenyl)-7-chloro-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid (310 mg) was added to 920 mg of N,N-dimethylformamide together with 220 mg of benzoic anhydride, which was stirred at 70° C. for 2 hours and at 100° C. for 2.5 hours. The reaction solution was combined with 50 ml of chloroform and 150 ml of distilled water. The solution was separated, the chloroform layer was dried over anhydrous magnesium sulfate and concentrated in vacua. Ethanol (6 ml) was added to the residue, which was allowed to stand. The precipitate was collected by filtration and washed with ethanol and then with diisopropyl ether to give 184 mg of the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05910498 |
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| Quelldatensatz | uspto-grants-1999_06 |
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| ORD ID | ord-5903198be8b94c9f9f8299525f10c662 |
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| Quellennotiz | uspto-grants-1999_06 |
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