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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207972Generated: October 30, 2026

Morpholine → HCID 118432114, compound

https://huagongshe.com/reaction/2207972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 118431899HCID 118431899—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 118432114HCID 11843211421.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

5-(3-Bromo-phenyl)-1-(2,4-difluoro-phenyl)-3-pentafluoroethyl-4,5-dihydro-1H-pyrazole (30.0 mg, 0.07 mmol) prepared in Step 2 of Preparation 5, morpholine (17.2 mg, 0.20 mmol), Pd2(dba)3 (3.0 mg, cat.), BINAP (4.1 mg, cat.) and sodium t-butoxide (9.5 mg, 0.10 mmol) were added to toluene (1.0 mL). The reaction mixture was stirred at 100° C. for 12 hours and then filtered through celite pad. A saturated solution of ammonium chloride was added to the filtrate, which was then extracted with ethyl acetate three times. The combined extract was washed with brine, dried on anhydrous magnesium sulfate, and then concentrated under reduced pressure to give a yellow liquid residue. The resulting residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/2) to give 7.0 mg of the titled compound as a yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376420B2
Source datasetuspto-grants-2016_06
ORD IDord-0aaeebe414bb49f08f1059667157f08f
Source noteuspto-grants-2016_06