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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239475Generated: October 31, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25005984, compound

https://huagongshe.com/reaction/2239475

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 68408168HCID 68408168—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25005984HCID 2500598433.1%

Reaction Steps

According to general procedure B, 4-Bromo-N,N-dimethyl-2-trifluoromethoxy-benzenesulfonamide (209 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,N-dimethyl-2-(trifluoromethoxy)benzenesulfonamide (73 mg, 32%) was provided after purification. MS (ESI) m/z 373. HPLC purity 99.1% at 210-370 nm, 9.7 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-b7aa68a3919e4a9ba64151adebd4ce52
Source noteuspto-grants-2010_05