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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110263Generated: October 30, 2026

Iodine → HCID 178506566, compound

https://huagongshe.com/reaction/2110263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantHCID 178526903HCID 178526903—
ProductHCID 178506566HCID 178506566—

Reaction Steps

In step 1 of Scheme A, nitroindazole compound a is treated with iodine or iodine equivalent to form 3-iodo indazole compound b. The amine functionality at the 1-position may be protected (not shown) prior to carrying out this step, and then subsequently deprotected. In step 2 the iodoindazole b is reacted with aryl boronic acid c in the presence of suitable palladium catalyst to afford 3-aryl indazole d. Aryl boronic acid c may in certain embodiments be replaced with a corresponding heteroaryl boronic acid. In step 3 the nitro group on indazole compound d is reduced to yield amino-substituted indazole e. Indazole e in step 4 is then treated with arylsulfonyl chloride f to form the sulfonamide compound g, Compound g is a compound of formula Ia in accordance with the invention.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517901B2
Source datasetuspto-grants-2009_04
ORD IDord-765a451d8b9141bba8606b829738ba36
Source noteuspto-grants-2009_04