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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919137Generated: November 1, 2026

4-(6-Nitropyridin-3-yl)-3-oxopiperazine-1-carboxylic acid tert-butyl ester → Tert-butyl 4-(6-aminopyridin-3-yl)-3-oxopiperazine-1-carboxylate

https://huagongshe.com/reaction/1919137

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(6-Nitropyridin-3-yl)-3-oxopiperazine-1-carboxylic acid tert-butyl esterHCID 59290952—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductTert-butyl 4-(6-aminopyridin-3-yl)-3-oxopiperazine-1-carboxylateHCID 5929095995.2%

Reaction Steps

To a solution of 332b (1.1 g, 3.4 mmol) in methanol (20 mL) was added Pd/C (10%) (250 mg). After three cycles of vacuum/H2 flash, the mixture was stirred under H2 at room temperature for 10 h. The mixture was filtered and the filtrate was evaporated in vacuo to afford 332c (946 mg, 95%), which was used for the next step without further purification. MS: [M+H]+ 293.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618107B2
Source datasetuspto-grants-2013_12
ORD IDord-aa6fbf9fa6e842c49aa56e9a6a53ec46
Source noteuspto-grants-2013_12