HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopentylamine → 4-(2-Bromo-acetyl)-N-cyclopentyl-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopentylamine | HCID 2906 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(2-bromoacetyl)benzenesulfonyl Chloride | HCID 2756834 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(2-Bromo-acetyl)-N-cyclopentyl-benzenesulfonamide | HCID 86616439 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
4-(2-Bromo-acetyl)-benzenesulfonyl chloride (150 mg, 0.17 mmol) was dissolved in 4 mL of dry dichloromethane. To this solution at 0° C., was added triethylamine (0.03 mL, 0.2 mmol), followed by cyclopentylamine (0.2 mmol, 0.011 g). Reaction mixture was stirred at 0° C. for 15 minutes and then quenched with H2O. The reaction mixture was extracted with H2O. The organic phase was isolated, dried over MgSO4 and evaporated. It was used in the next step without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07595398B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-61fd7bb351d74546ab036ec16a3e0970 |
| Source note | uspto-grants-2009_09 |