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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593579Generated: October 30, 2026

Bromide ion → HCID 16037646, compound

https://huagongshe.com/reaction/1593579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantTetrahydrofuranHCID 8028—
ReactantCyanamideHCID 9864—
ReactantPotassium CarbonateHCID 11430—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
Reactant(5-cyano-1-methyl-1H-pyrrol-2-yl)boronic acidHCID 11708078—
ProductHCID 16037646HCID 1603764616%

Reaction Steps

4-bromo-3-methoxyphenyl)cyanamide (0.113 g, 0.5 mmol) tris (dibenzylideneacetone) dipalladium (11.6 mg, 0.0126 mmol), N-methyl-5-cyanopyrroleboronic acid (0.150 g, 1 mmol), and potassium carbonate (0.276 g, 2 mmol) were placed in a 40 mL vial fitted with a septa. The vial was then filled with a continuous flow of nitrogen and THF (2 mL) was added with stirring. Tri-tert-butylphosphine (10 wt % in hexane) (0.0486 mL, 0.0252 mmol) was added to the mixture and allowed to stir until the starting bromide was consumed. The mixture was then diluted with 1/1 hexane/ethylacetate, filtered through a plug of silica gel, solvent evaporated and the residue was flash chromatographed on silica gel using 4/1 Hexane/THF to give [4-(5-cyano-1-methyl-1H-pyrrol-2-yl)-3-methoxyphenyl]cyanamide (0.020 g, 16%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07297713B2
Source datasetuspto-grants-2007_11
ORD IDord-2865e18f71e9450988c12fadeb7dfbaa
Source noteuspto-grants-2007_11