HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13425Erstellt: 23. Oktober 2026
Picolinic acid → N-(3-fluoro-4-(3-methyl-3-butenoyl)phenyl)pyridine-2-carboxamide
https://huagongshe.com/de/reaction/13425
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Picolinic acid | HCID 1018 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | N-(3-fluoro-4-((methoxy(methyl)amino)carbonyl)phenyl)pyridine-2-carboxamide | HCID 23145523 | — |
| Edukt | HCID 178448200 | HCID 178448200 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | N-(3-fluoro-4-(3-methyl-3-butenoyl)phenyl)pyridine-2-carboxamide | HCID 23145243 | — |
Reaktionsschritte
9.89 ml of (2-methyl-2-propen-1-yl)magnesium chloride (0.50 M tetrahydrofuran solution) was added to a tetrahydrofuran (10 ml) solution of 500 mg of N-(3-fluoro-4-((methoxy(methyl)amino)carbonyl)phenyl)pyridine-2-carboxamide obtained in the same method as in Example 145 (step 3) or in accordance with the method or by combining it with an ordinary method but using pyridine-2-carboxylic acid, with cooling with ice. The reaction liquid was stirred for 3 hours with cooling with ice, and then water was poured into the reaction solution, extracted with ethyl acetate and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=3/1) to obtain the entitled compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07728025B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-9581c41b61054aff8661bb529241a2ff |
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| Quellennotiz | uspto-grants-2010_06 |
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