HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Diisopropylethylamine → n-(2-{4-[(2r)-2-Hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl]piperazinyl}ethyl)[4-(trifluoromethyl)phenyl]carboxamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 5-(((R)-oxiran-2-yl)methoxy)-2-methylbenzo[d]thiazole | HCID 21023606 | — |
| Edukt | n-(2-Piperazinylethyl)[4-(trifluoromethyl)phenyl]carboxamide | HCID 21060632 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | n-(2-{4-[(2r)-2-Hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl]piperazinyl}ethyl)[4-(trifluoromethyl)phenyl]carboxamide | HCID 21060624 | — |
Reaktionsschritte
To a solution of N-(2-piperazinylethyl)[4-(trifluoromethyl)phenyl]carboxamide (0.2 g, 0.38 mmol) in ethanol was added diisopropyl ethylamine (0.25 ml, 1.5 mmol) and 5-[((2R)oxiran-2-yl)methoxy]-2-methylbenzothiazole (0.09 g, 0.42 mmol). The reaction was heated to 85 degrees for four hours. The mixture was then concentrated in vacuo and purified using preparative thin layer chromatography (10:1 DCM:MeOH) to yield N-(2-{4-[(2R)-2-hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl]piperazinyl}ethyl)[4-(trifluoromethyl)phenyl]carboxamide (M+1=523.0).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07262198B2 |
| Quelldatensatz | uspto-grants-2007_08 |
| ORD ID | ord-c0f3f4c58e1e4df3b47e4b37d9fa034c |
| Quellennotiz | uspto-grants-2007_08 |