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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239467Generated: October 31, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25005979, compound

https://huagongshe.com/reaction/2239467

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—
Reactant4-Bromo-N-(cyclopropylmethyl)-2-fluorobenzenesulfonamideHCID 68483200—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25005979HCID 2500597910.2%

Reaction Steps

According to general procedure B, 4-bromo-N-(cyclopropylmethyl)-2-fluorobenzenesulfonamide (181 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-(cyclopropylmethyl)-2-fluorobenzenesulfonamide (20 mg, 10%) was provided after purification. MS (ESI) m/z 333. HPLC purity 100.0% at 210-370 nm, 11.4 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-acc1143cfd584d06a1bc7a046fba770b
Source noteuspto-grants-2010_05