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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269897Generated: October 31, 2026

Ammonium formate → N-piperidin-3-yl-1H-indazol-5-amine

https://huagongshe.com/reaction/1269897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantN-(1-benzylpiperidin-3-yl)-1H-indazol-5-amineHCID 9857714—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN-piperidin-3-yl-1H-indazol-5-amineHCID 2293342674%

Reaction Steps

To a solution of the N-(1-benzylpiperidin-3-yl)-1H-indazol-5-amine (463 mg, 1.51 mmol) obtained in Example 535 in ethanol (10 ml) were added 10% Pd—C (50 mg) and then ammonium formate (952 mg, 15.1 mmol), and the resulting mixture was heated under reflux for 2 hours. The solid was removed by filtration using Celite, and the solvent was distilled off under reduced pressure. Chloroform/aqueous ammonia was added to the residue, followed by extraction with chloroform, and the extract solution was washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate, and then distilled under reduced pressure to remove the solvent, whereby N-piperidin-3-yl-1H-indazol-5-amine (241 mg, 74%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199147B2
Source datasetuspto-grants-2007_04
ORD IDord-faa6a980f3ec43b0b4e196a82dc98515
Source noteuspto-grants-2007_04