HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → N-(3-amino-2-methylpropyl)-4-cyanobenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 86729742 | HCID 86729742 | — |
| Product | N-(3-amino-2-methylpropyl)-4-cyanobenzenesulfonamide | HCID 86729743 | 65.6% |
Reaction Steps
A solution of the compound obtained in Step 1 (273 mg, 0.77 mmol) in TFA (1 mL, 12.98 mmol) was stirred at room temperature for min, and the mixture was concentrated under reduced pressure. To the residue were added ethyl acetate and 1N aqueous sodium hydroxide solution, and the organic layer was separated. The organic layer was washed with water and saturated brine, and dried, and the solvent was evaporated under reduced pressure to give N-(3-amino-2-methylpropyl)-4-cyanobenzenesulfonamide (128 mg, 0.505 mmol, 65.4%) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120776B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-afeae13304ce47a6bbd456ef5cc0c1ba |
| Source note | uspto-grants-2015_09 |