HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Riluzole → 3(2H)-Benzothiazoleethanol, 2-imino-6-(trifluoromethoxy)-, monohydrobromide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Riluzole | HCID 5070 | — |
| Edukt | 2-Bromoethanol | HCID 10898 | — |
| Edukt | 3-(2-Hydroxyethyl)-2-imino-6-trifluoromethoxybenzothiazoline | HCID 3076252 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 3(2H)-Benzothiazoleethanol, 2-imino-6-(trifluoromethoxy)-, monohydrobromide | HCID 3076251 | — |
Reaktionsbedingungen
| Temperatur | 20 °C |
|---|
Reaktionsschritte
3-(2-Hydroxyethyl)-2-imino-6-trifluoromethoxybenzothiazoline may be prepared in the following manner: 2-amino-6-trifluoromethoxybenzothiazole (9.4 g) and 2-bromoethanol (10 g) in absolute ethanol (30 cc) are heated for 95 hours to boiling. The mixture is cooled to a temperature in the region of 20° C. The precipitate formed is filtered off and washed with ethyl ether (100 cc). 3-(2-Hydroxyethyl)-2-imino-6-trifluoromethoxybenzothiazoline hydrobromide (6.4 g), m.p. 219° C., is thereby obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05008280 |
| Quelldatensatz | uspto-grants-1991_04 |
| ORD ID | ord-93dd34b74fbb4f82beac53e36185ee27 |
| Quellennotiz | uspto-grants-1991_04 |