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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239394Generated: October 31, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25004250, compound

https://huagongshe.com/reaction/2239394

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 60824558HCID 60824558—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25004250HCID 2500425014%

Reaction Steps

According to general procedure B, 4-bromo-N-ethyl-N-methylbenzenesulfonamide (111 mg, 0.40 mmol), 5-cyano-1-methyl-1H-pyrrol-2-ylboronic acid (72 mg, 0.48 mmol), potassium fluoride (76 mg, 1.3 mmol), and tris(dibenzylideneacetone)dipalladium(0) (10 mg, 0.01 mmol) were placed in an oven dried flask under nitrogen and dry THF (1.0 mL) was added. Tri-t-butylphosphine (60 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-ethyl-N-methylbenzenesulfonamide (17 mg, 14%) was provided after purification. MS (ESI) m/z 303. HPLC purity 99.5% at 210-370 nm, 10.3 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-86e09b959f484853a213bb614a3a8eba
Source noteuspto-grants-2010_05