HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine → 2-cyano-N-ethylbenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | 2-Cyanobenzenesulfonyl Chloride | HCID 522347 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-cyano-N-ethylbenzenesulfonamide | HCID 7303050 | 49.9% |
Reaction Steps
To 2-cyanobenzene-1-sulfonyl chloride (201 mg, 1.00 mmol) in THF (10 mL), a 2M THF solution of ethylamine (5.0 mL, 10.0 mmol) was added. After stirring for 30 min, the reaction was concentrated then purified via preparative HPLC eluting with MeOH/H2O/TFA to provide 2-cyano-N-ethylbenzenesulfonamide (105 mg). The product was dissolved in MeOH (8 mL), conc. HCl (70 mg) was added, and the whole was hydrogenated at 30 psi for 3 h. The reaction was filtered and dried (Na2SO4) to provide 201A (123 mg, 49%). LC-MS: 215.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07456195B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-687ef267f08440049c0a8627d0f5cd15 |
| Source note | uspto-grants-2008_11 |