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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055572Generated: November 3, 2026

3-(1,2,3,6-Tetrahydropyridin-4-yl)-1H-indole → HCID 11417818, compound

https://huagongshe.com/reaction/2055572

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(1,2,3,6-Tetrahydropyridin-4-yl)-1H-indoleHCID 2761023—
ReactantHCID 22326634HCID 22326634—
ProductHCID 11417818HCID 11417818—

Reaction Steps

2-{4-[4-(1H-Indol-3-yl)-3,6-dihydro-2H-pyridin-1-yl]-butyl}-2H-[1,2,4]triazolo[4,3-a]pyridin-3-one was prepared by reacting 2-(4-Chloro-butyl)-2H-[1,2,4]triazolo[4,3-a]pyridin-3-one (225 mg, 1 mmol) and 3-(1,2,3,6-Tetrahydro-pyridin-4-yl)-1H-indole (198 mg, 1 mmol) by adopting the procedure as outlined in Experimental 24. Yield: 87 mg (22%) compound was isolated as pale yellow solid. Mp: 123.2° C.; M+388.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332506B2
Source datasetuspto-grants-2008_02
ORD IDord-12664cd848ab44f9989c32231388ae90
Source noteuspto-grants-2008_02