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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2208074Generated: October 31, 2026

Dimethylformamide → HCID 118431992, compound

https://huagongshe.com/reaction/2208074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium CarbonateHCID 10340—
Reactant2-Acetylphenylboronic acidHCID 2734309—
ReactantHCID 118431811HCID 118431811—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventEthyl AcetateHCID 8857—
ProductHCID 118431992HCID 11843199223.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

5-(6-Bromo-pyridin-3-yl)-1-(2-chloro-phenyl)-3-[di-(trifluoromethyl)-hydroxy-methyl]-4,5-dihydro-1H-pyrazole (20.0 mg, 0.04 mmol) prepared in Step 4 of Preparation 20, 2-acetylphenylboronic acid (8.0 mg, 0.05 mmol), Pd(dppf)Cl2 (3.0 mg, cat.), and a 2N sodium carbonate solution (0.4 mL) were added to N,N-dimethylformamide (0.4 mL). The reaction mixture was stirred at 100° C. for 16 hours and then ethyl acetate was added thereto. The reaction mixture was washed with distilled water and 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=2/1) to give 5.0 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-6640aa260af746a8bb5ddc28c632146b
Source noteuspto-grants-2016_06