HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-5-chlorobenzenesulphonamide → (E)-5-chloro-2-(2-(4-chloro-2-methoxyphenyl)vinylsulfonamido)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-5-chlorobenzenesulphonamide | HCID 12295550 | — |
| Reactant | (E)-2-(4-chloro-2-methoxyphenyl)ethenesulfonyl chloride | HCID 22711054 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | (E)-5-chloro-2-(2-(4-chloro-2-methoxyphenyl)vinylsulfonamido)benzenesulfonamide | HCID 57751036 | 99.5% |
Reaction Steps
A solution of 2-amino-5-chlorobenzenesulfonamide (0.041 g, 0.20 mmol) and (E)-2-(4-chloro-2-methoxyphenyl)ethenesulfonyl chloride (0.053 g, 0.20 mmol) in pyridine (2 mL) was stirred at room temperature over night. The reaction mixture was concentrated, 1 M hydrochloric acid was added and the mixture was extracted with dichloromethane. The organic phase was dried over magnesium sulfate and the solvent was evaporated to give 0.087 g (99% yield) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09145380B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-da650443174d438fba1de736f5cb837b |
| Source note | uspto-grants-2015_09 |