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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706715Generated: October 29, 2026

1-(3-((4-nitro-1H-indazol-1-yl)methyl)piperidin-1-yl)ethanone → 1-(3-((4-amino-1H-indazol-1-yl)methyl)piperidin-1-yl)ethanone

https://huagongshe.com/reaction/706715

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-((4-nitro-1H-indazol-1-yl)methyl)piperidin-1-yl)ethanoneHCID 67974591—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product1-(3-((4-amino-1H-indazol-1-yl)methyl)piperidin-1-yl)ethanoneHCID 67976300100.6%

Reaction Steps

A solution of 1-(3-((4-nitro-1H-indazol-1-yl)methyl)piperidin-1-yl)ethanone (0.022 g, 0.073 mmol) in MeOH (1 mL) was purged with Argon, treated with 10% palladium on carbon (0.002 g) purged with more Argon, and then attached to a hydrogen balloon. The mixture was stirred at ambient temperature overnight, filtered through glass fiber filter paper, washed with MeOH and concentrated to give 1-(3-((4-amino-1H-indazol-1-yl)methyl)piperidin-1-yl)ethanone (0.020 g, 100% yield) as an amber oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174981B2
Source datasetuspto-grants-2015_11
ORD IDord-c61bb48d1db644839f175bdbbad22d1c
Source noteuspto-grants-2015_11