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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239465Generated: November 1, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25005978, compound

https://huagongshe.com/reaction/2239465

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-2-fluorobenzene-1-sulfonamideHCID 53439926—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25005978HCID 2500597824%

Reaction Steps

According to general procedure B, 4-bromo-N-cyclopropyl-2-fluorobenzenesulfonamide (176 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-2-fluorobenzenesulfonamide (45 mg, 24%) was provided after purification. MS (ESI) m/z 319. HPLC purity 100.0% at 210-370 nm, 8.7 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-6c871b5fa8bd48ca94178817d081f1b6
Source noteuspto-grants-2010_05