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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227305Generated: October 25, 2026

Iodine → HCID 178452228, compound

https://huagongshe.com/reaction/227305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPotassium HydroxideHCID 14797—
Reactanttert-Butyl 4-(1H-indazol-4-yl)piperazine-1-carboxylateHCID 44242883—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 178452228HCID 17845222835%

Reaction Steps

A solution of 4-[4-(t-butoxycarbonyl)piperazin-1-yl]-1H-indazole (5.00 g, 16.5 mmol) in N,N-dimethylformamide is treated with powdered potassium hydroxide (1.85 g, 33.07 mmol) and iodine (4.61 g, 18.2 mmol), stirred at room temperature for 16 h, diluted with ethyl acetate and quenched with 15% aqueous sodium metabisulfite. The phases are separated and the aqueous phase is extracted with ethyl acetate. The extracts and the organic phase are combined, washed with brine, dried over sodium sulfate and concentrated in vacuo to afford a crude solid. This solid is purified by column chromatography (silica gel, 10:90 to 15:85 to 20:80 ethyl acetate/hexanes) to afford the title product as a yellow solid, 2.40 g (35% yield) identified by HNMR and mass spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560470B2
Source datasetuspto-grants-2009_07
ORD IDord-4b81eb6fe753470185be2a6e02c3dcae
Source noteuspto-grants-2009_07