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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktBistrifluoroacetoxyiodobenzeneHCID 12041285—
EduktN-Methoxy-N-methyl-1H-indazole-3-carboxamideHCID 16036867—
EduktSodium BisulfiteHCID 23665763—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-iodo-N-methoxy-N-methyl-1H-indazole-3-carboxamideHCID 2058073872%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822478B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-8661c5eb07474683b1435d57239cbbd1
Quellennotizuspto-grants-2014_09