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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495368Generated: October 29, 2026

3-(4-Piperidinyl)-1H-indole → HCID 11233763, compound

https://huagongshe.com/reaction/495368

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-Piperidinyl)-1H-indoleHCID 702235—
ReactantHCID 11428752HCID 11428752—
ReactantHCID 19745981HCID 19745981—
ProductHCID 11233763HCID 11233763—

Reaction Steps

2-{2-[4-(1H-Indol-3-yl)-piperidin-1-yl]-ethyl}-2H-[1,2,4]triazolo[4,3-a]pyridin-3-one was prepared in a similar fashion to of 2-{2-[4-(1H-Indol-3-yl)-3,6-dihydro-2H-pyridin-1-yl]-ethyl}-2H-[1,2,4]triazolo[4,3-a]pyridin-3-one (example 22) using of toluene-4-sulfonic acid 2-(3-oxo-[1,2,4]triazolo[4,3-a]pyridin-2-yl)-ethyl ester and 3-Piperidin-4-yl-1H-indole. Yield: 70 mg of compound was obtained (39%). mp: 142° C.; M+: 362.1; H-NMR: 8.14 (b, 1H, NH), 7.74 (m, 1H), 7.62 (m, 1H), 7.35(m, 1H), 7.08 (m, 5H), 6.94 (m, 1H), 6.45 (m, 1H), 4.23 (m, CH2), 3.13 (d, CH2), 2.93 (m, CH2), 2.82 (m, 1H) 2.28 (t, CH2), 2.04(m, CH2), 1.86(m, CH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939870B2
Source datasetuspto-grants-2005_09
ORD IDord-6813d8ffb82244c691c03f8048fe7948
Source noteuspto-grants-2005_09