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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239463Generated: October 30, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25005625, compound

https://huagongshe.com/reaction/2239463

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 68482644HCID 68482644—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25005625HCID 2500562513%

Reaction Steps

According to general procedure B, 4-bromo-2-fluoro-N-isopropylbenzenesulfonamide (177 mg, 0.59 mmol), 5-cyano-1-methyl-1H-pyrrol-2-ylboronic acid (106 mg, 0.70 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-fluoro-N-isopropylbenzenesulfonamide (24 mg, 13%) was provided after purification. MS (ESI) m/z 321. HPLC purity 100.0% at 210-370 nm, 9.0 min.; the Xterrag 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-273a9b0533574015ba5887f58c19afc8
Source noteuspto-grants-2010_05