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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2208001Generated: November 2, 2026

Butane → HCID 118431733, compound

https://huagongshe.com/reaction/2208001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButaneHCID 7843—
ReactantSodium CarbonateHCID 10340—
ReactantTert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine-1-carboxylateHCID 4642098—
ReactantHCID 118431774HCID 118431774—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
ProductHCID 118431733HCID 11843173359%

Reaction Conditions

Temperature88 °C

Reaction Steps

5-(5-Bromo-2-fluoro-phenyl)-1-(2,4-difluoro-phenyl)-3-pentafluoroethyl-4,5-dihydro-1H-pyrazole (500.0 mg, 1.06 mmol) prepared in Step 5 of Preparation 8, 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,6-dihydro-2H-pyridin-1-carboxylic acid tert-butyl ester (26.7 mg, 1.59 mmol), Pd(PPh3)4 (123.0 mg, cat.) and a 2N sodium carbonate solution (5.0 mL) were added to a mixed solvent of ethanol (5.0 mL) and 1,2-dimethylethane (20.0 mL). The reaction mixture was stirred at 88° C. for 2 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=1/15) to give 360.0 mg of the titled compound as a white liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376420B2
Source datasetuspto-grants-2016_06
ORD IDord-23c6adedd49241c38cec86ec3d2cadb8
Source noteuspto-grants-2016_06