HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopropylamine → N-Cyclopropyl 3-bromo-5-trifluoromethylbenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | 3-Bromo-5-(trifluoromethyl)benzenesulfonyl chloride | HCID 2778610 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-Cyclopropyl 3-bromo-5-trifluoromethylbenzenesulfonamide | HCID 26986221 | — |
Reaction Steps
3-Bromo-5-(trifluoromethyl)benzenesulfonyl chloride (0.2 g, 0.62 mmol) is added to a solution of cyclopropylamine (0.09 μl, 1.3 mmol) in DCM (5 ml), and the resulting solution is stirred at room temperature overnight. The reaction mixture is diluted with DCM (2×10 ml), washed with 0.1M HCl (5 ml), sat. aq. NaHCO3 (5 ml), dried (MgSO4) and concentrated in vacuo to yield the title compound. 1H NMR (400 MHz, d6-DMSO) δ 8.37 (1H, s), 8.23 (1H, s), 8.06 (1H, s), 2.21-2.17 (1H, m), 0.55-0.50 (2H, m) 0.40-0.36 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846687B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-e87ab9b6205a45d48a44f373460a0fb3 |
| Source note | uspto-grants-2014_09 |