Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2208055Generated: November 1, 2026

tert-Butyl piperazine-1-carboxylate → HCID 118431826, compound

https://huagongshe.com/reaction/2208055

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 118431805HCID 118431805—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 118431826HCID 11843182639.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

5-(4-Bromo-phenyl)-1-(2-chloro-phenyl)-3-[di-(trifluoromethyl)-hydroxy-methyl]-4,5-dihydro-1H-pyrazole (1.0 g, 1.99 mmol) prepared in Step 4 of Preparation 17, 1-BOC-piperazine (557.0 mg, 2.99 mmol), Pd2(dba)3 (91.0 mg, cat.), BINAP (124.0 mg, cat.) and sodium t-butoxide (287.0 mg, 2.99 mmol) were added to toluene (20.0 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=1/4) to give 480.0 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-e4cd0db90cec4a339ae08779138094d4
Source noteuspto-grants-2016_06