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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239495Generated: October 30, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25006738, compound

https://huagongshe.com/reaction/2239495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantPotassium FluorideHCID 522689—
Reactant(5-cyano-1-methyl-1H-pyrrol-2-yl)boronic acidHCID 11708078—
ReactantHCID 59443491HCID 59443491—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25006738HCID 2500673815.4%

Reaction Steps

According to general procedure B, 4-bromo-2,5-difluoro-N-methylbenzenesulfonamide (143 mg, 0.5 mmol), 5-cyano-1-methyl-1H-pyrrol-2-ylboronic acid (90 mg, 0.60 mmol), potassium fluoride (96 mg, 1.65 mmol), and tris(dibenzylideneacetone)dipalladium (12 mg, 0.013 mmol) were placed in an oven dried flask under nitrogen and dry THF (1.3 mL) was added. Tri-t-butylphosphine (75 μL, 0.026 mmol, 10 wt % in hexane) was added and the reaction was stirred for 16 hours. Purification afforded 4-(5-cyano-1-methyl-1H-pyrrol-2-yl)-2,5-difluoro-N-methylbenzenesulfonamide (24 mg). HPLC purity 87.6% at 210-370 nm, 8.4 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. HRMS: calcd for C13H11F2N3O2S−H+, 310.04673; found (ESI-FTMS, [M−H]−1), 310.04692

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723332B2
Source datasetuspto-grants-2010_05
ORD IDord-61dad2b2af8740629f5ddb181ce0bc17
Source noteuspto-grants-2010_05