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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-(3-Aminophenyl)-1-phenylmethanesulfonamide | HCID 16772451 | — |
| Reactant | 2-Chloro-5-(isoquinolin-6-yl)oxazole | HCID 71060582 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | N-(3-((5-(isoquinolin-6-yl)oxazol-2-yl)amino)phenyl)-1-phenylmethanesulfonamide | HCID 71060600 | 72.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08865709B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-00be5cf6391b449cacd22ed468717474 |
|---|
| Source note | uspto-grants-2014_10 |
|---|