Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456422Generated: October 25, 2026

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

https://huagongshe.com/reaction/456422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantTetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
Reactant(R)-Octahydro-pyrido[1,2-a]pyrazineHCID 773775—
ReactantPyridazine, 3-chloro-6-[4-(trifluoromethyl)phenyl]-HCID 12449554—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
Product(R)-2-[6-(4-Trifluoromethyl-phenyl)-pyridazin-3-yl]-octahydro-pyrido[1,2-a]pyrazineHCID 2079906398.1%

Reaction Conditions

Temperature160 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186721B2
Source datasetuspto-grants-2007_03
ORD IDord-bfd189a0842d47fd8b77df7eb5d727b1
Source noteuspto-grants-2007_03