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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68919Generated: October 26, 2026

Iodine → 5-iodo-N-methoxy-N-methyl-1H-indazole-3-carboxamide

https://huagongshe.com/reaction/68919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantBistrifluoroacetoxyiodobenzeneHCID 12041285—
ReactantN-Methoxy-N-methyl-1H-indazole-3-carboxamideHCID 16036867—
ReactantSodium BisulfiteHCID 23665763—
SolventDichloromethaneHCID 6344—
Product5-iodo-N-methoxy-N-methyl-1H-indazole-3-carboxamideHCID 2058073872%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822478B2
Source datasetuspto-grants-2014_09
ORD IDord-8661c5eb07474683b1435d57239cbbd1
Source noteuspto-grants-2014_09