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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218459Generated: October 27, 2026

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

https://huagongshe.com/reaction/218459

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 a solution of N-methoxy-N-methyl-1H-indazole-3-carboxamide (12.4 g, 60.42 mmol) in CH2Cl2 (200 mL) was added bis(trifluoroacetoxy)iodobenzene (28.78 g, 66.74 mmol), followed by dropwise addition of iodine (9.22 g, 36.33 mmol) in CH2Cl2 at rt. The reaction was stirred overnight, after which 300 mL saturated NaHSO3 was added and a solid began to precipitate, which was then filtered. The filtrate was concentrated and triturated with a small amount of CH2Cl2. The combined solids were dried to give 5-iodo-N-methoxy-N-methyl-1H-indazole-3-carboxamide (14.4 g, 72%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198456B2
Source datasetuspto-grants-2012_06
ORD IDord-bf0c526919e04f2bb8dbe14fc2f2e7db
Source noteuspto-grants-2012_06