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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239455Generated: October 31, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25005621, compound

https://huagongshe.com/reaction/2239455

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—
Reactant4-Bromo-N-cyclopropyl-3-fluorobenzenesulfonamideHCID 68481397—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25005621HCID 2500562114%

Reaction Steps

According to general procedure B, 4-bromo-N-cyclopropyl-3-fluorobenzenesulfonamide (175 mg, 0.59 mmol), 5-cyano-1-methyl-1H-pyrrol-2-ylboronic acid (106 mg, 0.70 mmol), potassium fluoride (113 mg, 1.95 mmol), and tris(dibenzylideneacetone)dipalladium(0) (15 mg, 0.01 mmol) were placed in an oven dried flask under nitrogen and dry THF (1.4 mL) was added. Tri-t-butylphosphine (89 μL, 0.02 mmol, 10 wt % in hexane) was added and the reaction was stirred for 16 hours. 4-(5-cyano-1-methyl-1H-pyrrol-2-yl)-N-cyclopropyl-3-fluorobenzenesulfonamide (26 mg, 14%) was provided after purification. MS (ESI) m/z 319. HPLC purity 100.0% at 210-370 nm, 8.9 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-6eaf70bed2ad4fdfa524a6917e2a8c25
Source noteuspto-grants-2010_05