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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33239Generated: October 24, 2026

HCID 178418260, compound → HCID 178470417, compound

https://huagongshe.com/en/reaction/33239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178418260HCID 178418260—
ReactantHCID 178470418HCID 178470418—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
CatalystTetraethylammonium cyanideHCID 3014735—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDimethylformamideHCID 6228—
ProductHCID 178470417HCID 178470417—

Reaction Conditions

Temperature120 °C

Reaction Steps

1.57 g (4.5 mmol) of 4-Iodo-5-thiophen-2-yl-2H-pyrazole-3-carboxylic acid ethyl ester, 0.81 g (9.0 mmol) of copper cyanide and 352 mg (2.3 mmol) of tetraethylammonium cyanide were dissolved in 10 ml of DMF and 20 ml of tetrahydrofuran and the solution was degassed with argon. 223 mg (0.2 mmol) of Tris(dibenzylideneacetone)dipalladium (0) and 374 mg (0.7 mmol) of 1,1′-bis-(diphenylphosphino) ferrocene were added at RT. The reaction was stirred at 120° C. for 5 h. The solvent was removed under reduced pressure. The residue was dissolved in ethyl acetate and this solution was washed with saturated aqueous sodium bicarbonate. The organic phase was dried with sodium sulfate, filtered and the solvent was removed under reduced pressure. The product was purified by silica gel chromatography eluting with n-heptane:ethyl acetate/1:1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429581B2
Source datasetuspto-grants-2008_09
ORD IDord-0f32fbdb35bc46b399bc692733142482
Source noteuspto-grants-2008_09