HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Triethylamine → N-{1-[2-(1H-Indol-3-yl)ethyl]piperidin-4-yl}methanesulfonamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Methanesulfonyl chloride | HCID 31297 | — |
| Edukt | 4-Piperidinamine, 1-(2-(1H-indol-3-yl)ethyl)-, hydrate | HCID 215415 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-{1-[2-(1H-Indol-3-yl)ethyl]piperidin-4-yl}methanesulfonamide | HCID 22754838 | 105,7% |
Reaktionsschritte
To 3-[2-(4-Amino-1-piperidyl)ethyl]indole (1.307 g.) suspended in a solution of triethylamine (2 mls.) in dichloromethane (10 mls.) at room temperature with stirring was added methane sulphonyl chloride (0.570 g.) in dichloromethane (5 mls.). After stirring for 18 hours the solution was washed with water and the organic phase separated, dried and evaporated to yield the title compound (1.690 g.) as an oil. This was recrystallised from ethanolic hydrogen chloride as the hydrochloride salt (0.560 g., m.p. 241°-242° C.).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04034098 |
| Quelldatensatz | uspto-grants-1977_07 |
| ORD ID | ord-1c0fc56b21124a86b1764bb51ba8f5f9 |
| Quellennotiz | uspto-grants-1977_07 |