Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9498Generated: October 29, 2026

N-[2-(7-bromo-3-nitroquinolin-4-ylamino)ethyl]methanesulfonamide → N-[2-(3-amino-7-bromoquinolin-4-ylamino)ethyl]methanesulfonamide

https://huagongshe.com/reaction/9498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[2-(7-bromo-3-nitroquinolin-4-ylamino)ethyl]methanesulfonamideHCID 21984316—
CatalystPlatinumHCID 23939—
SolventAcetonitrileHCID 6342—
ProductN-[2-(3-amino-7-bromoquinolin-4-ylamino)ethyl]methanesulfonamideHCID 21984309—

Reaction Steps

An 8 L stainless steel Parr vessel was charged with N-[2-(7-bromo-3-nitroquinolin-4-ylamino)ethyl]methanesulfonamide (61 g), 5% Pt/C catalyst (6.0 g) and acetonitrile (3 L). The vessel was evacuated, filled with hydrogen (45 psi, 3.1×105 Pa), and shaken at ambient temperature overnight. The reaction mixture was filtered through CELITE filter agent and concentrated under reduced pressure to provide N-[2-(3-amino-7-bromoquinolin-4-ylamino)ethyl]methanesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091214B2
Source datasetuspto-grants-2006_08
ORD IDord-b33109869e254d76aed04997a8636ff6
Source noteuspto-grants-2006_08