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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239492Generated: November 1, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25006737, compound

https://huagongshe.com/reaction/2239492

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 68481888HCID 68481888—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25006737HCID 2500673719%

Reaction Steps

According to general procedure B, 4-bromo-N-tert-butyl-2-(trifluoromethoxy)benzenesulfonamide (225 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. N-tert-butyl-4-(5-cyano-1-methyl-1H-pyrrol-2-yl)-2-(trifluoromethoxy)benzenesulfonamide (44 mg, 19%) was provided after purification. MS (ESI) m/z 401. HPLC purity 99.0% 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-94fb391e77654b939a34a98ae78f76ee
Source noteuspto-grants-2010_05