HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Toluenesulfonylhydrazide → 5-Chloro-2-(2-(4-chloro-2-methoxyphenyl)ethylsulfonamido)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Toluenesulfonylhydrazide | HCID 15303 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | (E)-5-chloro-2-(2-(4-chloro-2-methoxyphenyl)vinylsulfonamido)benzenesulfonamide | HCID 57751036 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Chloro-2-(2-(4-chloro-2-methoxyphenyl)ethylsulfonamido)benzenesulfonamide | HCID 57750961 | 44.3% |
Reaction Conditions
| Temperature | 180 °C |
|---|
Reaction Steps
Sodium acetate (64 mg, 0.78 mmol) and para-toluenesulfonhydrazide (145 mg, 0.78 mmol) was added to a solution of (E)-5-chloro-2-(2-(4-chloro-2-methoxyphenyl)vinylsulfonamido)benzenesulfonamide (85 mg, 0.19 mmol) in tetrahydrofuran (3 mL). The reaction mixture was heated at 180° C. for 15 min in a microwave reactor. The solids were removed by filtration, washed with tetrahydrofuran and the combined filtrates were evaporated. Purification by preparative HPLC gave 0.037 g (43% 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-fc816705ef4d4e9db6e79c8753557056 |
| Source note | uspto-grants-2015_09 |