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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2208018Generated: November 1, 2026

tert-Butyl piperazine-1-carboxylate → HCID 118431818, compound

https://huagongshe.com/reaction/2208018

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 118431855HCID 118431855—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 118431818HCID 11843181894.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

5-(4-Bromo-pyridin-2-yl)-1-(2,4-difluoro-phenyl)-3-pentafluoroethyl-4,5-dihydro-1H-pyrazole (300.0 mg, 0.66 mmol) prepared in Step 4 of Preparation 11, 1-BOC-piperazine (184.0 mg, 0.99 mmol), Pd2(dba)3 (30.2 mg, cat.), BINAP (41.1 mg, cat.) and sodium t-butoxide (114.0 mg, 1.19 mmol) were added to toluene (10.0 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=1/3) to give 350.0 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-febdd16580c24bc5844fd981a3e435a6
Source noteuspto-grants-2016_06