HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Cyanobenzenesulphonamide → 4-cyano-N-[({2-[4-(2-ethyl-4-phenyl-1H-imidazol-1-yl)phenyl]ethyl}amino)carbonyl]benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Cyanobenzenesulphonamide | HCID 76566 | — |
| Reactant | 2-[4-(2-ethyl-4-phenyl-1H-imidazol-1-yl)phenyl]ethylcarbamate | HCID 22291350 | — |
| Product | 4-cyano-N-[({2-[4-(2-ethyl-4-phenyl-1H-imidazol-1-yl)phenyl]ethyl}amino)carbonyl]benzenesulfonamide | HCID 22291395 | — |
Reaction Steps
The title compound was prepared according to the procedure described in step 2 of Example 18 from 2-[4-(2-ethyl-4-phenyl-1H-imidazol-1-yl)phenyl]ethylcarbamate and 4-cyanobenzenesulfonamide. MS (ESI) m/z 500 [M+H]+, 498 [M−H]−, 1H-NMR (DMSO-d6) δ 1.14 (3H, t, J=7.5 Hz), 2.61 (2H, q, J=7.5 Hz), 2.72 (2H, t, J=7.1 Hz), 3.10-3.30 (2H, m), 6.60 (1H, br), 7.19 (1H, t, J=7.1 Hz), 7.28-7.39 (6H, m), 7.70 (1H, s), 7.78 (2H, d, J=7.1 Hz), 8.00-8.08 (4H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06956050B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-b80c72395def4bf9869ba13d178ca21e |
| Source note | uspto-grants-2005_10 |