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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239412Generated: November 3, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25004587, compound

https://huagongshe.com/reaction/2239412

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 60643547HCID 60643547—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25004587HCID 2500458742%

Reaction Steps

According to general procedure B, 4-bromo-N-(2,2,2-trifluoroethyl)benzenesulfonamide (127 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-(2,2,2-trifluoroethyl)benzenesulfonamide (57 mg, 42%) was provided after purification. MS (ESI) m/z 343. HPLC purity 97.2% at 210-370 nm, 10.1 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-2160445d524a46e2827e587faddd9cf7
Source noteuspto-grants-2010_05