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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239459Generated: October 30, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25005623, compound

https://huagongshe.com/reaction/2239459

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 68484532HCID 68484532—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25005623HCID 2500562314.2%

Reaction Steps

According to general procedure B, 4-bromo-N-cyclobutyl-3-fluorobenzenesulfonamide (182 mg, 0.59 mmol), 5-cyano-1-methyl-1H-pyrrol-2-ylboronic acid (106 mg, 0.70 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-3-fluorobenzenesulfonamide (28 mg, 14%) was provided after purification. HRMS: calcd for C16H16FN3O2S−H+, 332.08745; found (ESI, [M−H]−), 332.0867. HPLC purity 96.9% at 210-370 nm, 9.4 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-1dd74d348c834c58a3464a3e0ddd29ed
Source noteuspto-grants-2010_05