HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-tert-Butyl-4-((3-fluoro-4-methoxybenzylidene)amino)benzenesulfonamide → N-tert-butyl-4-[5-(4-ethoxyphenyl)imidazol-1-yl]benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-tert-Butyl-4-((3-fluoro-4-methoxybenzylidene)amino)benzenesulfonamide | HCID 11132250 | — |
| Reactant | N-tert-Butyl-4-[(4-ethoxybenzylidene)amino]benzenesulfonamide | HCID 69032410 | — |
| Product | N-tert-butyl-4-[5-(4-ethoxyphenyl)imidazol-1-yl]benzenesulfonamide | HCID 12988041 | 77% |
Reaction Steps
Following a similar process to that described in example 3, but starting from N-tert-butyl-4-[(4-ethoxybenzylidene)amino]benzenesulfonamide (obtained in example 6) instead of from N-tert-butyl-4-[(3-fluoro-4-methoxybenzylidene)amino]benzenesulfonamide, the title compound is obtained in 77% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351836B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-10e8d0f772f5418b8e4255595b14dd59 |
| Source note | uspto-grants-2008_04 |