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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239388Generated: October 31, 2026

4-Bromo-N-propylbenzenesulfonamide → HCID 25004246, compound

https://huagongshe.com/reaction/2239388

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-N-propylbenzenesulfonamideHCID 77027—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantPotassium FluorideHCID 522689—
Reactant(5-cyano-1-methyl-1H-pyrrol-2-yl)boronic acidHCID 11708078—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25004246HCID 2500424617.3%

Reaction Steps

According to general procedure B, 4-bromo-N-propylbenzenesulfonamide (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-propylbenzenesulfonamide (21 mg, 17%) was provided after purification. MS (ESI) m/z 303. HPLC purity 100.0% at 210-370 mn, 10.2 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-f10ae640d80b43aea0f4256b03e736b7
Source noteuspto-grants-2010_05