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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714998Generated: October 30, 2026

tert-butyl 4-nitro-1H-pyrazole-1-carboxylate → tert-butyl 4-amino-1H-pyrazole-1-carboxylate

https://huagongshe.com/reaction/714998

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-nitro-1H-pyrazole-1-carboxylateHCID 66765764—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-butyl 4-amino-1H-pyrazole-1-carboxylateHCID 5958764895.7%

Reaction Steps

A solution of tert-butyl 4-nitro-1H-pyrazole-1-carboxylate (1.0 g, 4.7 mmol) in MeOH (120 ml) was passed through the H-Cube with full hydrogen mode at 60° C. and 1 bar with a 10% Pd/C cartridge using 1 ml/min flow rate. The solution was then passed through the H-Cube for a second time using identical conditions and the solvent removed in vacuo to afford tert-butyl 4-amino-1H-pyrazole-1-carboxylate (0.82 g, 4.5 mmol, 95%). 1H NMR (DMSO) δ 1.54 (9H, s), 4.42 (2H, s), 7.33 (1H, s), 7.35 (1H, s). LCMS (2) Rt: 1.45 min; m/z (ES+) 206 M+Na+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187465B2
Source datasetuspto-grants-2015_11
ORD IDord-0dca8df094df40cead42b1814cf91325
Source noteuspto-grants-2015_11