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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373883Generated: November 1, 2026

tert-butyl N'-(3-nitroquinolin-4-yl)hydrazinecarboxylate → tert-butyl N'-(3-aminoquinolin-4-yl)hydrazinecarboxylate

https://huagongshe.com/reaction/1373883

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N'-(3-nitroquinolin-4-yl)hydrazinecarboxylateHCID 21075824—
CatalystPalladiumHCID 23938—
SolventIsopropanolHCID 3776—
Producttert-butyl N'-(3-aminoquinolin-4-yl)hydrazinecarboxylateHCID 2107582396.7%

Reaction Steps

A suspension of tert-butyl N′-(3-nitroquinolin-4-yl)hydrazinecarboxylate (2.50 g, 8.22 mmol) in 150 mL of isopropanol was treated with 1.0 g of 10% palladium on carbon and the mixture was shaken under an atmosphere of hydrogen (3.8×105 Pa) for 2 h. The reaction mixture was then filtered through a pad of CELITE filter agent and rinsed with isopropanol, and the filtrate was concentrated under reduced pressure to give tert-butyl N′-(3-aminoquinolin-4-yl)hydrazinecarboxylate (2.18 g) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163947B2
Source datasetuspto-grants-2007_01
ORD IDord-fe49ac0531914bc391effe0326644a53
Source noteuspto-grants-2007_01