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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239429Generated: October 30, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25004923, compound

https://huagongshe.com/reaction/2239429

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 47304372HCID 47304372—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25004923HCID 2500492333%

Reaction Steps

According to general procedure B, 4-bromo-N-propyl-2-(trifluoromethyl)benzenesulfonamide (193 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)-N-propyl-2-(trifluoromethyl)benzenesulfonamide (68 mg, 33%) was provided after purification. MS (ESI) m/z 371. HPLC purity 100.0% at 210-370 nm, 10.7 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-32ba19f6c8b04c2c81a5af98c8661978
Source noteuspto-grants-2010_05