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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239441Generated: October 30, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25005263, compound

https://huagongshe.com/reaction/2239441

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 68481117HCID 68481117—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25005263HCID 2500526331%

Reaction Steps

According to general procedure B, 4-bromo-3-fluoro-N-methylbenzenesulfonamide (158 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 (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)-3-fluoro-N-methylbenzenesulfonamide (53 mg, 31%) was provided after purification. HRMS: calcd for C13H12FN3O2S, 293.06342; found (EI, M+.), 293.0627. HPLC purity 99.5% at 210-370 nm, 8.2 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-d99d329acc6b4dc392ca4792a6098d8f
Source noteuspto-grants-2010_05