Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269730Generated: October 30, 2026

Trifluoroacetic acid → 5-(piperidin-4-yloxy)-1H-indazole

https://huagongshe.com/reaction/1269730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 22933993HCID 22933993—
SolventDichloromethaneHCID 6344—
Product5-(piperidin-4-yloxy)-1H-indazoleHCID 2293346752.1%

Reaction Steps

Trifluoroacetic acid (0.20 ml, 2.60 mmol) was added to a solution of tert-butyl 4-(1H-indazol-5-yloxy)-1-piperidinecarboxylate (70 mg, 0.221 mmol) in methylene chloride (5 ml) at room temperature and stirred overnight at room temperature. Then, the solvent of the reaction solution was distilled off under reduced pressure and the resulting residue was poured into a 1N-aqueous sodium hydroxide solution and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 5-(4-piperidinyloxy)-1H-indazole (25 mg, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199147B2
Source datasetuspto-grants-2007_04
ORD IDord-22dda2d220934c559cbf99cceb0641b1
Source noteuspto-grants-2007_04