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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354570Generated: November 1, 2026

Iodine → HCID 59381950, compound

https://huagongshe.com/reaction/2354570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium hydrideHCID 24758—
ReactantHCID 59381926HCID 59381926—
SolventDimethylformamideHCID 6228—
ProductHCID 59381950HCID 5938195087.4%

Reaction Steps

To a solution of 3-benzyl-4-(1H-indol-5-yl)-piperazine-1-carboxylic acid tert-butyl ester (0.17 g, 0.4 mmol) in 2.5 mL DMF was added powdered KOH (0.060 g, 1.1 mmol), followed by I2 (0.11 g, 0.4 mmol) in DMF. The solution was stirred for 45 minutes and then treated with 10% aqueous Na2S2O3. The mixture was extracted with EtOAc, and the combined organic layers were dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was immediately taken up in 2 mL DMF and treated with 60% NaH (0.02 g, 0.5 mmol). After 20 minutes the solution was treated with benzenesulfonyl chloride (0.07 mL, 0.5 mmol). After 30 minutes of stirring the mixture was quenched with H2O and extracted with EtOAc. The combined organic layers were washed with H2O, washed with brine, dried over MgSO4, filtered, and concentrated under reduced pressure. Purification via flash chromatography (30% EtOAc in hexanes) afforded 4-(1-benzenesulfonyl-3-iodo-1H-indol-5-yl)-3-benzyl-piperazine-1-carboxylic acid tert-butyl ester (0.23 g, 83%) as a white foam; MS (M+H)=658.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754721B2
Source datasetuspto-grants-2010_07
ORD IDord-4b58b8709cbc48829120680130075e4b
Source noteuspto-grants-2010_07