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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 456422Erstellt: 25. Oktober 2026

Diisopropylethylamine → (R)-2-[6-(4-Trifluoromethyl-phenyl)-pyridazin-3-yl]-octahydro-pyrido[1,2-a]pyrazine

https://huagongshe.com/reaction/456422

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktTetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
Edukt(R)-Octahydro-pyrido[1,2-a]pyrazineHCID 773775—
EduktPyridazine, 3-chloro-6-[4-(trifluoromethyl)phenyl]-HCID 12449554—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelDichloromethaneHCID 6344—
Produkt(R)-2-[6-(4-Trifluoromethyl-phenyl)-pyridazin-3-yl]-octahydro-pyrido[1,2-a]pyrazineHCID 2079906398,1%

Reaktionsbedingungen

Temperatur160 °C

Reaktionsschritte

A mixture of the dihydrochloride salt of (R)-octahydropyrido[1,2-a]pyrazine (649 mg, 3.05 mmol), diisopropylethylamine (1.17 ml, 6.72 mmol), 3-chloro-6-(4-trifluoromethylphenyl)-pyridazine (290 mg, 1.12 mmol) and dimethylsulfoxide (1 ml) was heated in a closed vessel at 160° C. for 40 min. The reaction mixture was cooled to room temperature, diluted with dichloromethane (10 ml) and washed with water (2×15 ml) and brine (15 ml). The organic layer was dried over magnesium sulphate. The solvent was removed in vacuo to give 398 mg of the title compound as the free base.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07186721B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-bfd189a0842d47fd8b77df7eb5d727b1
Quellennotizuspto-grants-2007_03