HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1943985Erstellt: 26. Oktober 2026
Ammonia → 5-Fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxamide
https://huagongshe.com/reaction/1943985
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ammonia | HCID 222 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | 5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxylic acid | HCID 57431513 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 5-Fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxamide | HCID 66845696 | — |
Reaktionsschritte
To a suspension, stirred at 20° C., of 2 g (6.96 mmol) of 5-fluoro-1-[(3-fluorophenyl)-methyl]-1H-indole-2-carboxylic acid, prepared in step 1.1, in 80 mL of dry toluene are added 5.08 mL (69.62 mmol) of thionyl chloride. The reaction mixture is refluxed for 2 hours with stirring and is then concentrated under reduced pressure. The resulting product is taken up in 10 mL of dichloromethane, and this solution is poured dropwise into a solution of 9.12 mL (69.62 mmol) of 30% aqueous ammonia. The reaction mixture is stirred for 14 hours at 20° C. After this time, a solid is collected by filtration, and is triturated in 50 mL of diisopropyl ether. After filtering off and drying under reduced pressure, 0.58 g of the expected product is collected.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08394820B2 |
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| Quelldatensatz | uspto-grants-2013_03 |
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| ORD ID | ord-0c95923f5a964156bd34107648a0327a |
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| Quellennotiz | uspto-grants-2013_03 |
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