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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239416Generated: October 31, 2026

Potassium Fluoride → HCID 25004589, compound

https://huagongshe.com/reaction/2239416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
Reactant1-(4-Bromophenylsulfonyl)-1H-pyrroleHCID 5108932—
Reactant(5-cyano-1-methyl-1H-pyrrol-2-yl)boronic acidHCID 11708078—
CatalystTris(1,1-dimethylethyl)phosphineHCID 83681—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25004589HCID 2500458954.2%

Reaction Steps

According to general procedure B, 1-[(4-bromophenyl)sulfonyl]-1H-pyrrole (250 mg, 0.87 mmol), 5-cyano-1-methyl-1H-pyrrol-2-ylboronic acid (72 mg, 0.48 mmol), potassium fluoride (76 mg, 1.3 mmol), and tris(dibenzylideneacetone)dipalladium(0) (10 mg, 0.01 mmol) were placed in an oven dried flask under nitrogen and dry THF (1.0 mL) was added. Tri-t-butylphosphine (60 μL, 0.02 mmol, 10 wt % in hexane) was added and the reaction was stirred for 16 hours. 1-methyl-5-[4-(1H-pyrrol-1-ylsulfonyl)phenyl]-1H-pyrrole-2-carbonitrile (81 mg, 30%) was provided after purification. MS (ESI) m/z 311. HPLC purity 100.0% at 210-370 nm, 11.6 min.; the Xterra® RP18 column, 3.5μ, 150×4.6 mm column, 1.2 mL/min., 85/15-5/95 (ammonium formate buffer pH=3.5/ACN+MeOH) for 10 min., hold 4 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723332B2
Source datasetuspto-grants-2010_05
ORD IDord-b2fdc8aba78642d5a6d52e422db8af30
Source noteuspto-grants-2010_05