Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363630Generated: October 28, 2026

1-[(3-Nitroquinolin-4-ylamino)methyl]cyclohexanol → 1-[(3-Aminoquinolin-4-ylamino)methyl]cyclohexanol

https://huagongshe.com/reaction/1363630

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[(3-Nitroquinolin-4-ylamino)methyl]cyclohexanolHCID 57457808—
SolventEthyl AcetateHCID 8857—
Product1-[(3-Aminoquinolin-4-ylamino)methyl]cyclohexanolHCID 57457825—

Reaction Steps

A suspension of 1-{[(3-nitroquinolin-4-yl)amino]methyl}cyclohexanol (15.0 g, 49.8 mmol) in ethyl acetate (225 mL) in a Parr vessel was purged with nitrogen; 5% platinum on carbon (1.5 g) was added. The reaction was placed under hydrogen pressure (35 psi, 2.4×105 Pa) for 3.5 hours and then filtered through a layer of CELITE filter agent. The filter cake was washed with ethyl acetate (100 mL), and the filtrate was concentrated under reduced pressure to provide 1-{[(3-aminoquinolin-4-yl)amino]methyl}cyclohexanol as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884207B2
Source datasetuspto-grants-2011_02
ORD IDord-cb0e49cae87f42d98dbe4180cf8a0664
Source noteuspto-grants-2011_02