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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234077Generated: October 30, 2026

Ethyl Acetate → 2-(3-Methoxy-6-pyridin-4-yl-pyridazin-4-yl)-3-vinyl-1H-indole

https://huagongshe.com/reaction/2234077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTributylvinyltinHCID 81998—
ReactantPotassium FluorideHCID 522689—
Reactant3-Iodo-2-(3-methoxy-6-pyridin-4-yl-pyridazin-4-yl)-1H-indoleHCID 23102914—
CatalystTetraethylammonium ChlorideHCID 5946—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
Product2-(3-Methoxy-6-pyridin-4-yl-pyridazin-4-yl)-3-vinyl-1H-indoleHCID 23092509—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 430 mg 3-Iodo-2-(3-methoxy-6-pyridin-4-yl-pyridazin-4-yl)-1H-indole, 490 mg tributyl(vinyl)tin, 165 mg tetraethylammonium-chloride and 35 mg bis(triphenylphosphine)palladium(II) chloride in DMF is stirred at 80° C. for 40 min. After cooling to room temperature, 15 ml aqueous potassium fluoride solution (30%) are added and the mixture stirred for 30 min at room temperature before extraction with EtOAc. The organic layer is dried over MgSO4 and the solvent evaporated ion prior to purification of the crude product by preparative RP-HPLC eluting with a gradient of 0-100% acetonitrile in water (+0.01% HCOOH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709466B2
Source datasetuspto-grants-2010_05
ORD IDord-61e7c4e3c5674bd895217371c6e2f765
Source noteuspto-grants-2010_05