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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239406Generated: November 1, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25004585, compound

https://huagongshe.com/reaction/2239406

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 25044868HCID 25044868—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25004585HCID 2500458516%

Reaction Steps

According to general procedure B, 4-bromo-N-cyclobutylbenzenesulfonamide (117 mg, 0.40 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. 4-(5-cyano-1-methyl-1H-pyrrol-2-yl)-N-cyclobutylbenzenesulfonamide (20 mg, 16%) was provided after purification. MS (ESI) m/z 315. HPLC purity 98.8% at 210-370 nm, 10.4 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723332B2
Source datasetuspto-grants-2010_05
ORD IDord-177fe01ed75f4173ae8f8d95bbdf1b7e
Source noteuspto-grants-2010_05