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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1889087Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1889087

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethyloxonium tetrafluoroborateHCID 2723982—
Edukt4-{[2-Chloro-3-(trifluoromethyl)phenyl]carbonyl}-2-piperazinoneHCID 66599208—
EduktHCID 67970623HCID 67970623—
LösungsmittelDichloromethaneHCID 6344—
Produkt7-{[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]pyrazineHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08501946B2
Quelldatensatzuspto-grants-2013_08
ORD IDord-7a9964f64f7d4463a507c1a0c5f79960
Quellennotizuspto-grants-2013_08