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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537860Generated: October 26, 2026

N-(3-Aminophenyl)-1-phenylmethanesulfonamide → N-(3-((5-(isoquinolin-6-yl)oxazol-2-yl)amino)phenyl)-1-phenylmethanesulfonamide

https://huagongshe.com/reaction/537860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-Aminophenyl)-1-phenylmethanesulfonamideHCID 16772451—
Reactant2-Chloro-5-(isoquinolin-6-yl)oxazoleHCID 71060582—
SolventIsopropanolHCID 3776—
ProductN-(3-((5-(isoquinolin-6-yl)oxazol-2-yl)amino)phenyl)-1-phenylmethanesulfonamideHCID 7106060072.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-chloro-5-(isoquinolin-6-yl)oxazole 14 (0.069 g, 0.30 mmol) and N-(3-aminophenyl)-1-phenylmethanesulfonamide 26 (0.157 g, 0.599 mmol) in 2-propanol (20 mL) was heated to 80° C. for 24 h with stirring. Upon cooling, solvent was evaporated and silica column purified (Biotage) (Acetone/hexane as an eluent) to provide N-(3-((5-(isoquinolin-6-yl)oxazol-2-yl)amino)phenyl)-1-phenylmethanesulfonamide 27 (0.099 g, 72% yield) as pale yellow solid. MS (ES) m/z 457 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865709B2
Source datasetuspto-grants-2014_10
ORD IDord-00be5cf6391b449cacd22ed468717474
Source noteuspto-grants-2014_10