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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239449Generated: October 30, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25005267, compound

https://huagongshe.com/reaction/2239449

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 68482810HCID 68482810—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25005267HCID 2500526719%

Reaction Steps

According to general procedure B, 4-bromo-3-fluoro-N-isopropylbenzenesulfonamide (174 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)-3-fluoro-N-isopropylbenzenesulfonamide (35 mg, 19%) was provided after purification. HRMS: calcd for C15H16FN3O2S, 321.09472; found (EI, M+.), 321.0948. HPLC purity 100.0% 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-83eb2ecb0e1b4ea28ceb26452e4a7af8
Source noteuspto-grants-2010_05