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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269738Generated: October 30, 2026

Acetic Acid → 5-(4-benzyl-1-piperazinyl)-1H-indazole

https://huagongshe.com/reaction/1269738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantHCID 69430818HCID 69430818—
SolventTetrahydrofuranHCID 8028—
Product5-(4-benzyl-1-piperazinyl)-1H-indazoleHCID 2293378447.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

Acetic acid (2.6 ml) and water (0.7 ml) were added to a solution of 5-(4-benzyl-1-piperazinyl)-1-tetrahydro-2H-pyran-2-yl-1H-indazole (100 mg, 0.266 mmol) in tetrahydrofuran (1.3 ml) at room temperature and stirred 80° C. for 7 hours. Then, the reaction solution was concentrated and the resulting residue was diluted with ethyl acetate and washed with a saturated aqueous sodium hydrogencarbonate solution and then a saturated aqueous sodium chloride solution. The organic layer was dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent, and the resulting residue was purified by a thin-layer chromatography (eluent: chloroform/methanol=95/5) to obtain 5-(4-benzyl-1-piperazinyl)-1H-indazole (37 mg, 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199147B2
Source datasetuspto-grants-2007_04
ORD IDord-637009381bcf4269a8a1c5a5a670423a
Source noteuspto-grants-2007_04