HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Triethyloxonium tetrafluoroborate → 7-{[2-Chloro-3-(trifluoromethyl)phenyl]carbonyl}-3-(1,2,4-thiadiazol-5-yl)-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyrazine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| Edukt | 4-{[2-Chloro-3-(trifluoromethyl)phenyl]carbonyl}-2-piperazinone | HCID 66599208 | — |
| Edukt | HCID 67970623 | HCID 67970623 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 7-{[2-Chloro-3-(trifluoromethyl)phenyl]carbonyl}-3-(1,2,4-thiadiazol-5-yl)-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyrazine | HCID 66599293 | — |
Reaktionsschritte
To a solution of 4-{[2-chloro-3-(trifluoromethyl)phenyl]carbonyl}-2-piperazinone (I1) (0.307 g, 1 mmol) in dry Dichloromethane (DCM) (3 ml) was added triethyloxonium tetrafluoroborate (0.209 g, 1.100 mmol). The solution was then stirred at room temperature and under argon for 30 minutes. 1,2,4-Thiadiazole-5-carbohydrazide (I80) (0.144 g, 1.000 mmol) was then added and the solution was stirred for 1 hour, before the solvent was concentrated and n-BuOH (3.00 ml) was added. The solution was then stirred under argon and reflux for a further 3 hours. The solution was then allowed to cool to room temperature before the solvent was evaporated in vacuo.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08501946B2 |
| Quelldatensatz | uspto-grants-2013_08 |
| ORD ID | ord-7a9964f64f7d4463a507c1a0c5f79960 |
| Quellennotiz | uspto-grants-2013_08 |