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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239390Generated: November 2, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25004248, compound

https://huagongshe.com/reaction/2239390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantBenzenesulfonamide, p-bromo-N-isopropyl-HCID 121253—
ReactantPotassium FluorideHCID 522689—
Reactant(5-cyano-1-methyl-1H-pyrrol-2-yl)boronic acidHCID 11708078—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25004248HCID 2500424812.4%

Reaction Steps

According to general procedure B, 4-bromo-N-isopropylbenzenesulfonamide (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-isopropylbenzenesulfonamide (15 mg, 12%) was provided after purification. MS (ESI) m/z 303. HPLC purity 100.0% 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-bb914bce0a98410da8463ea70d1077b7
Source noteuspto-grants-2010_05