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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239404Generated: October 30, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 25004583, compound

https://huagongshe.com/reaction/2239404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
Reactant4-[(4-Bromobenzene)sulfonyl]morpholineHCID 253128—
ReactantPotassium FluorideHCID 522689—
Reactant(5-cyano-1-methyl-1H-pyrrol-2-yl)boronic acidHCID 11708078—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 25004583HCID 250045838.3%

Reaction Steps

According to general procedure B, 4-[(4-bromophenyl)sulfonyl]morpholine (122 mg, 0.40 mmol), 5-cyano-1-methyl-1H-pyrrol-2-ylboronic acid (72 mg, 0.48 mmol), potassium fluoride (76 mg, 1.3 mmol), and tris(dibenzylideneacetone)dipalladium(0) (10 mg, 0.01 mmol) were placed in an oven dried flask under nitrogen and dry THF (1.0 mL) was added. Tri-t-butylphosphine (60 μL, 0.02 mmol, 10 wt % in hexane) was added and the reaction was stirred for 16 hours. 1-methyl-5-[4-(morpholin-4-ylsulfonyl)phenyl]-1H-pyrrole-2-carbonitrile (11 mg, 8%) was provided after purification. MS (ESI) m/z 331. HPLC purity 100.0% 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-a0c6717a7b5a41749e5f561f9dbda04c
Source noteuspto-grants-2010_05