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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239431Generated: November 2, 2026

Potassium Fluoride → HCID 25004924, compound

https://huagongshe.com/reaction/2239431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
Reactant(5-cyano-1-methyl-1H-pyrrol-2-yl)boronic acidHCID 11708078—
ReactantHCID 68482537HCID 68482537—
CatalystTris(1,1-dimethylethyl)phosphineHCID 83681—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25004924HCID 2500492454.5%

Reaction Steps

In analogous manner to general procedure B, 1-{[4-bromo-2-(trifluoromethyl)phenyl]sulfonyl}pyrrolidine (200 mg, 0.56 mmol), 5-cyano-1-methyl-1H-pyrrol-2-ylboronic acid (100 mg, 0.67 mmol), potassium fluoride (107 mg, 1.85 mmol), and tris(dibenzylideneacetone)dipalladium(0) (14 mg, 0.01 mmol) were placed in an oven dried flask under nitrogen and dry THF (1.4 mL) was added. Tri-t-butylphosphine (83 μL, 0.02 mmol, 10 wt % in hexane) was added and the reaction was stirred for 16 hours. 1-methyl-5-[4-(pyrrolidin-1-ylsulfonyl)-3-(trifluoromethyl)phenyl]-1H-pyrrole-2-carbonitrile (117 mg, 54%) was provided after purification. HRMS: calcd for C17H16F3N3O2S+H+, 384.09881; found (ESI, [M+H]+), 384.0991, HPLC purity 100.0% at 210-370 nm, 10.9 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-20bd1d6f87c84e45be7e109f43a020c3
Source noteuspto-grants-2010_05