HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-{[4-(2-([(tert-butyl)amino]sulfonyl}phenyl)phenyl]carbonylamino}-5-chlorophenyl)-N-(5-chloro(2-pyridyl))carboxamide → N-(5-chloro(2-pyridyl))(5-chloro-2-([4-(2-sulfamoylphenyl)-phenyl]carbonylamino}phenyl)-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-{[4-(2-([(tert-butyl)amino]sulfonyl}phenyl)phenyl]carbonylamino}-5-chlorophenyl)-N-(5-chloro(2-pyridyl))carboxamide | HCID 131723193 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | N-(5-chloro(2-pyridyl))(5-chloro-2-([4-(2-sulfamoylphenyl)-phenyl]carbonylamino}phenyl)-carboxamide | HCID 22596297 | 25% |
Reaction Steps
The mixture of the compound of (2-{[4-(2-{[(tert-butyl)amino]sulfonyl}phenyl)phenyl]carbonylamino}-5-chlorophenyl)-N-(5-chloro(2-pyridyl))carboxamide example 12 (0.5 mmol) in trifluoroacetic acid (5 ml) was stirred at r.t. for 5 hrs. After the evaporation of solvent, the crude residue was purified by RP-HPLC to give N-(5-chloro(2-pyridyl))(5-chloro-2-{[4-(2-sulfamoylphenyl)-phenyl]carbonylamino}phenyl)-carboxamide as a white powder (68 mg, 25%). MS found for C25H18Cl2N4O4S M+=541, (M+2)+=543.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07727982B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-1e221f4018b74cbe910c2e2fc6fd7adf |
| Source note | uspto-grants-2010_06 |