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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239414Generated: November 3, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25004588, compound

https://huagongshe.com/reaction/2239414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantPotassium FluorideHCID 522689—
ReactantHCID 3845777HCID 3845777—
Reactant(5-cyano-1-methyl-1H-pyrrol-2-yl)boronic acidHCID 11708078—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25004588HCID 250045885%

Reaction Steps

According to general procedure B, 4-bromo-N-(cyclopropylmethyl)benzenesulfonamide (116 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-(cyclopropylmethyl)benzenesulfonamide (6 mg, 5%) was provided after purification. MS (ESI) m/z 315. HPLC purity 100.0% at 210-370 mn, 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-67812fbe48d4470b83ee99fbbd700a2e
Source noteuspto-grants-2010_05