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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069260Generated: October 28, 2026

Sodium Hydroxide → 3-(Piperazin-1-YL)-1H-indazole

https://huagongshe.com/reaction/1069260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 14823453HCID 14823453—
SolventSulfuric AcidHCID 1118—
Product3-(Piperazin-1-YL)-1H-indazoleHCID 1482344573%

Reaction Steps

A mixture of 4-(-1H-indazol-3yl)-1-piperazinecarbonitrile (8.0 g, 40 mmol) and 25% H2SO4 (100 ml) was stirred at reflux for 4.5 hours. The reaction was cooled in an ice bath and made basic by the dropwise addition of 50% NaOH. The basic solution was extracted with ethyl acetate. The ethyl acetate was washed with H2O, dried with MgSO4 and concentrated to afford 5.2 g (73% of the desired compound, as a solid. The solid was recrystallized twice from toluene to afford 3.0 g of 3-(1-piperazinyl)-1H-indazole, m.p.=153-155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251907B1
Source datasetuspto-grants-2001_06
ORD IDord-555523bcad994aac92a76323398fd744
Source noteuspto-grants-2001_06