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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269772Generated: October 30, 2026

Trifluoroacetic acid → benzyl 4-[(1H-indazol-5-ylamino)sulfonyl]piperidine-1-carboxylate

https://huagongshe.com/reaction/1269772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactantbenzyl 4-{[(1-tetrahydro-2H-pyran-2-yl-1H-indazol-5-yl)amino]sulfonyl}-1-piperidinecarboxylateHCID 69431167—
SolventDichloromethaneHCID 6344—
Productbenzyl 4-[(1H-indazol-5-ylamino)sulfonyl]piperidine-1-carboxylateHCID 1844721376.5%

Reaction Steps

Trifluoroacetic acid (5.0 ml) was added to a solution of benzyl 4-{[(1-tetrahydro-2H-pyran-2-yl-1H-indazol-5-yl)amino]sulfonyl}-1-piperidinecarboxylate (500 mg, 1.00 mmol) in methylene chloride (50 ml) at room temperature and stirred for 2 hours. After the reaction solution was concentrated, a saturated aqueous sodium hydrogencarbonate solution was added thereto, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and distilled under reduced pressure to remove the solvent, and resulting residue was purified by a silica gel column chromatography (eluent: chloroform/methanol=50/1) to obtain benzyl 4-[(1H-indazol-5-ylamino)sulfonyl]piperidine-1-carboxylate (317 mg, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199147B2
Source datasetuspto-grants-2007_04
ORD IDord-504c2dee442441f0862d322eeabd25b4
Source noteuspto-grants-2007_04