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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2208012Generated: October 31, 2026

tert-Butyl piperazine-1-carboxylate → 5-[3-(4-BOC-piperazin-1-yl)-pyridin-5-yl]-1-(2,4-difluoro-phenyl)-3-pentafluoroethyl-4,5-dihydro-1H-pyrazole

https://huagongshe.com/reaction/2208012

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
Reactant5-(3-bromo-pyridin-5-yl)-1-(2,4-difluoro-phenyl)-3-pentafluoroethyl-4,5-dihydro-1H-pyrazoleHCID 118431713—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product5-[3-(4-BOC-piperazin-1-yl)-pyridin-5-yl]-1-(2,4-difluoro-phenyl)-3-pentafluoroethyl-4,5-dihydro-1H-pyrazoleHCID 11843174352.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

5-(3-Bromo-pyridin-5-yl)-1-(2,4-difluoro-phenyl)-3-pentafluoroethyl-4,5-dihydro-1H-pyrazole (340.0 mg, 0.75 mmol) prepared in Step 4 of Preparation 10, 1-BOC-piperazine (208.0 mg, 1.12 mmol), Pd2(dba)3 (34.1 mg, cat.), BINAP (46.4 mg, cat.) and sodium t-butoxide (128.9 mg, 1.34 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 220.0 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-36c99e2a94704f508eab7f1f68012557
Source noteuspto-grants-2016_06