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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269773Generated: October 31, 2026

Ammonium formate → N-(1H-indazol-5-yl)piperidine-4-sulfonamide

https://huagongshe.com/reaction/1269773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactantbenzyl 4-[(1H-indazol-5-ylamino)sulfonyl]piperidine-1-carboxylateHCID 18447213—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN-(1H-indazol-5-yl)piperidine-4-sulfonamideHCID 2293360369%

Reaction Steps

Ammonium formate (250 mg) and 10%-Pd/C (50 mg) were added to a solution of benzyl 4-[(1H-indazol-5-ylamino)sulfonyl]piperidine-1-carboxylate (250 mg, 0.603 mmol) in ethanol (15 ml) at room temperature, and the resulting mixture was refluxed for 1 hour. The reaction mixture was filtered by the use of Celite, and the filtrate was concentrated and the resulting residue was dissolved in a mixture of chloroform and methanol, followed by adding thereto diethyl ether. The solid precipitated was collected by filtration and dried under reduced pressure to obtain N-(1H-indazol-5-yl)piperidine-4-sulfonamide (116 mg, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199147B2
Source datasetuspto-grants-2007_04
ORD IDord-c8e00c56e0114c83a60066a84584f961
Source noteuspto-grants-2007_04