Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239417Generated: November 2, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25004590, compound

https://huagongshe.com/reaction/2239417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantPotassium FluorideHCID 522689—
Reactant4-bromo-2-(trifluoromethyl)benzenesulfonamideHCID 2778392—
Reactant(5-cyano-1-methyl-1H-pyrrol-2-yl)boronic acidHCID 11708078—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25004590HCID 2500459018.4%

Reaction Steps

According to general procedure B, 4-bromo-2-(trifluoromethyl)benzenesulfonamide (170 mg, 0.56 mmol), 5-cyano-1-methyl-1H-pyrrol-2-ylboronic acid (100 mg, 0.67 mmol), potassium fluoride (107 mg, 1.85 mmol), and tris(dibenzylideneacetone)dipalladium(0) (14 mg, 0.01 mmol) were placed in an oven dried flask under nitrogen and dry THF (1.4 mL) was added. Tri-t-butylphosphine (83 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-(trifluoromethyl)benzenesulfonamide (34 mg, 18%) was provided after purification. MS (ESI) m/z 329. HPLC purity 98.6% at 210-370 nm, 9.1 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-25bdbef393ff4b049339a2e22e9f37f2
Source noteuspto-grants-2010_05