Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630472Generated: October 31, 2026

Diisopropylethylamine → HCID 59242655, compound

https://huagongshe.com/reaction/1630472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3,5-Difluorobenzyl bromideHCID 518896—
ReactantHCID 24880031HCID 24880031—
SolventAcetonitrileHCID 6342—
ProductHCID 59242655HCID 5924265553.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-phenyl-6-piperazin-1-yl-3-trifluoromethyl-pyridazine (E1) (0.050 g, 0.16 mmol), 3,5-difluorobenzyl bromide (0.031 ml, 0.24 mmol) and diisopropylethylamine (0.056 ml, 0.32 mmol) in acetonitrile (2 ml) was stirred at 100° C. for 10 min., under microwave irradiation. The solvent was evaporated in vacuo and then, dichloromethane and ammonium chloride (10% aqueous solution) were added. The mixture was filtered through a diatomaceous earth cartridge. The solvent was then evaporated in vacuo and the residue was purified by CC-TLC (centrifugal circular thin-layer chromatography) on a chromatotron (a preparative, centrifugally accelerated, radial, thin-layer chromatograph). The crude product was crystallised from diethyl ether/heptane to yield E3 (0.037 g, 52%) as a solid. C22H19F5N4 requires 434; Found 435 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791120B2
Source datasetuspto-grants-2014_07
ORD IDord-14538d9e14e44d719055dadf3f7cab65
Source noteuspto-grants-2014_07