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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239493Generated: November 3, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25006739, compound

https://huagongshe.com/reaction/2239493

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 68477957HCID 68477957—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25006739HCID 2500673914.3%

Reaction Steps

According to general procedure B, 4-bromo-2-(dimethylamino)-N,N-dimethylbenzenesulfonamide (180 mg, 0.59 mmol), 5-cyano-1-methyl-1H-pyrrol-2-ylboronic acid (107 mg, 0.71 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)-2-(dimethylamino)-N,N-dimethylbenzenesulfonamide (28 mg, 14%) was provided after purification. MS (ESI) m/z 332. HPLC purity 100.0% at 210-370 nm, 9.4 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-df4501bb8fd84dd39bb40ea53b642fb9
Source noteuspto-grants-2010_05