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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613352Generated: October 29, 2026

Indole → HCID 22349913, compound

https://huagongshe.com/reaction/613352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
Reactant4-AminopyridineHCID 1727—
ReactantOxalyl chlorideHCID 65578—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22349913HCID 22349913—

Reaction Steps

A solution of 10 g (85.3 mmol) of indole in 100 ml of ether is added dropwise at 0° C. to a solution of 9 ml of oxalyl chloride in 100 ml of anhydrous ether. The mixture is kept under reflux for 3 hours. A suspension of 12 g (127.9 mmol) of 4-aminopyridine in 500 ml of tetrahydrofuran is then added dropwise at -5° C., and the reaction mixture is heated to reflux temperature with stirring for 3 hours and allowed to stand overnight at room temperature. The precipitate is filtered and treated with water and the dried compound is purified on a silica gel column (silica gel 60, Merck AG, Darmstadt) using the eluent methylene chloride/ethanol (10:1, v/v).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008231
Source datasetuspto-grants-1999_12
ORD IDord-84d6bcd946c847529560149799a168e2
Source noteuspto-grants-1999_12