HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 58724166, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chlorobenzenesulfonyl chloride | HCID 76187 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 62389644 | HCID 62389644 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58724166 | HCID 58724166 | — |
Reaction Steps
Ethyl 1-(piperazin-1-yl)cyclobutanecarboxylate (0.71 mmol) was dissolved in CH2Cl2 (5 ml). Triethylamine (0.30 ml, 2.1 mmol), followed by 2-chlorobenzenesulfonyl chloride (0.11 ml, 0.79 mmol), was added at room temperature. The orange-colored solution was stirred at room temperature for 6 h before saturated NaHCO3 solution was added. The mixture was extracted twice with EtOAc. Combined organic layers were washed once with brine, dried over MgSO4, filtered and concentrated. The crude product was purified by column chromatography (SiO2, gradient 5-10% Et2O/CH2Cl2) to give ethyl 1-(4-(2-chlorophenylsulfonyl)piperazin-1-yl)cyclobutanecarboxylate as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07759339B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-d31bd8a72ab645348bfec9dd24aab8d9 |
| Source note | uspto-grants-2010_07 |