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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637985Generated: October 29, 2026

1-(Benzenesulfonyl)-3-(4-methylpiperazin-1-yl)-1H-indazole → 3-(4-Methylpiperazin-1-yl)-1H-indazole

https://huagongshe.com/reaction/1637985

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Benzenesulfonyl)-3-(4-methylpiperazin-1-yl)-1H-indazoleHCID 14823425—
ReactantHCID 178418582HCID 178418582—
SolventMethanolHCID 887—
Product3-(4-Methylpiperazin-1-yl)-1H-indazoleHCID 1482345280.3%

Reaction Steps

A stirred mixture of 3-(4-methyl-1-piperazinyl)-1-phenylsulfonyl-1H-indazole (13.5 g, 38 mmol), methanol (150 ml) and 25% CH3ONa in methanol (15.3 ml) was stirred and refluxed for 2.5 hours. The reaction was concentrated to about one-tenth its volume, and water was added to the mixture, resulting in a red solution. The solution was extracted with dichloromethane, the extract washed (H2O), dried (MgSO4), and the solvent was concentrated to afford 6.6 g of a rose-colored solid. Two recrystallizations from toluenehexane afforded 4.3 g (52%) of 3-(4-methyl-1-piperazinyl)-1H-indazole as an off-white solid, m.p.=111-113° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06043240
Source datasetuspto-grants-2000_03
ORD IDord-6a8ff4c7fe8d40099f1b751465213688
Source noteuspto-grants-2000_03