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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515378Generated: October 27, 2026

tert-Butyl 4-(6-nitro-1H-indazol-1-yl)piperidine-1-carboxylate → tert-Butyl 4-(6-amino-1H-indazol-1-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/515378

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(6-nitro-1H-indazol-1-yl)piperidine-1-carboxylateHCID 68609514—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-Butyl 4-(6-amino-1H-indazol-1-yl)piperidine-1-carboxylateHCID 68272187147.5%

Reaction Steps

tert-Butyl 4-(6-nitro-1H-indazol-1-yl)piperidine-1-carboxylate (3.00 mmol, 1.04 g) and palladium (10% on C) (0.150 mmol, 0.160 g) in ethanol (30 mL) were stirred under a hydrogen atmosphere at 5 bar for 1 hour. The reaction mixture was filtered and concentrated at reduced pressure to afford the title compound (1.4 g). MS (ESI) m/z 317.2 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108939B2
Source datasetuspto-grants-2015_08
ORD IDord-22b95033f17b4419b262c531c1a65376
Source noteuspto-grants-2015_08