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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239490Generated: October 30, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25006736, compound

https://huagongshe.com/reaction/2239490

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 68485410HCID 68485410—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25006736HCID 2500673624%

Reaction Steps

According to general procedure B, 4-bromo-N-cyclobutyl-2-(trifluoromethoxy)benzenesulfonamide (224 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)-N-cyclobutyl-2-(trifluoromethoxy)benzenesulfonamide (56 mg, 24%) was provided after purification. MS (ESI) m/z 399. HPLC purity 99.4% at 210-370 nm, 10.0 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-48c3c0653022415f9762e920e1c84084
Source noteuspto-grants-2010_05