HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 68919Erstellt: 24. Oktober 2026
Iodine → 5-iodo-N-methoxy-N-methyl-1H-indazole-3-carboxamide
https://huagongshe.com/de/reaction/68919
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Iodine | HCID 807 | — |
| Edukt | Bistrifluoroacetoxyiodobenzene | HCID 12041285 | — |
| Edukt | N-Methoxy-N-methyl-1H-indazole-3-carboxamide | HCID 16036867 | — |
| Edukt | Sodium Bisulfite | HCID 23665763 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 5-iodo-N-methoxy-N-methyl-1H-indazole-3-carboxamide | HCID 20580738 | 72% |
Reaktionsschritte
To the N-methoxy-N-methyl-1H-indazole-3-carboxamide (IX) (20 g, 97.4 mmol) in 1 L DCM was added bis(trifluoroacetoxy)iodobenzene (46 g, 107 mmol) followed by portionwise addition of iodine (14.84 g, 58.5 mmol) at r.t. After 1 hour, 600 mL of saturated NaHSO3 was added and a solid began to precipitate which was filtered and rinsed with excess DCM. The filtrate was washed with brine, dried over MgSO4, concentrated and the remaining solid was triturated with a minimal amount of DCM. The combined solids were dried under vacuum over KOH to produce 5-iodo-N-methoxy-N-methyl-1H-indazole-3-carboxamide (X) as a white solid (23.2 g, 70 mmol, 72% yield). 1H NMR (DMSO-d6) δ ppm 3.45 (s, 4H), 3.77 (s, 4H), 7.45-7.54 (m, 1H), 7.66 (dd, J=8.81, 1.51 Hz, 1H), 8.40 (d, J=1.01 Hz, 1H); ESIMS found for C10H10IN3O2 m/z 331 (M+H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08822478B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-8661c5eb07474683b1435d57239cbbd1 |
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| Quellennotiz | uspto-grants-2014_09 |
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