HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-{2-[N-(5-chloro(2-pyridyl))carbamoyl](3-thienyl)}(4-(2-sulfamoylphenyl)phenyl]carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | HCID 22596369 | HCID 22596369 | — |
| Reactant | 3-Amino-2-(4-chloro-2-pyridinyl)aminocarbonyl thiophene | HCID 22601674 | — |
| Product | N-{2-[N-(5-chloro(2-pyridyl))carbamoyl](3-thienyl)}(4-(2-sulfamoylphenyl)phenyl]carboxamide | HCID 10229449 | — |
Reaction Steps
A solution of 4-(2-{[(tert-butyl)amino]sulfonyl}phenyl)benzoyl chloride (1 equiv), 3-amino-2-(4-chloro-2-pyridinyl)aminocarbonyl thiophene (1equiv), pyridine (5 equiv) in dichloromethane was stirred at rt overnight. The mixture was diluted with dichloromethane, washed with water, dried over Na2SO4, filtered and evaporated. The residue was refluxed with 1 mL of TFA for 2 h. After evaporation, reverse phase HPLC gave the title product. ES-MS 51 3(M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06376515B2 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-4306526713a144688c02a672150e7a50 |
| Source note | uspto-grants-2002_04 |