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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239471Generated: November 1, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25005982, compound

https://huagongshe.com/reaction/2239471

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—
Reactant749262-49-5HCID 46738066—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25005982HCID 2500598224.5%

Reaction Steps

According to general procedure B, 4-bromo-2-(trifluoromethoxy)benzenesulfonamide (192 mg, 0.59 mmol), 5-cyano-1-methyl-1H-pyrrol-2-ylboronic acid (107 mg, 0.71 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)-2-(trifluoromethoxy)benzenesulfonamide (50 mg, 24%) was provided after purification. MS (ESI) m/z 345. HPLC purity 100.0% at 210-370 nm, 8.4 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-14e0befed9344a7189890b889fc369de
Source noteuspto-grants-2010_05