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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292994Generated: October 25, 2026

Benzenesulfinic acid, sodium salt → HCID 178452229, compound

https://huagongshe.com/reaction/1292994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfinic acid, sodium saltHCID 2723840—
ReactantHCID 178452228HCID 178452228—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylformamideHCID 6228—
ProductHCID 178452229HCID 17845222918%

Reaction Conditions

Temperature125 °C

Reaction Steps

A mixture of 4-[4-(t-butoxycarbonyl)piperazin-1-yl]-3-iodo-1H-indazole (0.110 g, 0.257 mmol), sodium benzene sulfinate (0.068 g, 0.411 mmol), copper(I) iodide (0.073 g, 0.386 mmol) and N,N-dimethylformamide is added to a screw-capped test-tube with Teflon-lined septum. The tube is evacuated and backfilled with argon. This procedure is repeated twice, then the tube is heated to 125° C. for 4 h. The reaction mixture is cooled, partitioned between ethyl acetate and water and filtered through a pad of diatomaceous earth. The filtrate is separated. The organic phase is washed with brine, dried over sodium sulfate and concentrated in vacuo. The resulting crude material is purified by column chromatography (silica gel, 40:60 ethyl acetate/hexanes) to afford the title compound as a pale yellow foam, 0.022 g (18% yield), identified by NMR and mass spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238696B2
Source datasetuspto-grants-2007_07
ORD IDord-fd3f2ecc43624aef9247ea38a5a4a617
Source noteuspto-grants-2007_07