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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955674Generated: November 1, 2026

2-Chloropyridine → HCID 22277752, compound

https://huagongshe.com/reaction/1955674

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloropyridineHCID 7977—
Reactant1-AminoindoleHCID 643221—
ReactantPotassium tert-butoxideHCID 23665647—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 22277752HCID 22277752—

Reaction Steps

Potassium tert-butoxide (3.4 g) was added to a room temperature solution of N-aminoindole (2.0 g) in 1-methyl-2-pyrrolidinone (40 ml). After stirring for one hour, 2-chloropyridine (1.6 ml) was added and the resulting solution was stirred for forty-eight hours. The reaction mixture was then quenched with water, diluted with ethyl acetate (250 ml) and washed with brine (3×250 ml). The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo to give an oil. Purification of the residue by flash chromatography (silica, 0-5% ethyl acetate/dichloromethane) gave the title compound as a solid (2.0 g), m.p. 109°-110° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05776955
Source datasetuspto-grants-1998_07
ORD IDord-70f2173d38794e97825135364f862412
Source noteuspto-grants-1998_07