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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275722Generated: October 25, 2026

5-Chloro-1-[1-[2-(indan-2-yl)ethyl]-1,2,3,6-tetrahydropyridin-4-yl]-1H-indole → 5-Chloro-1-[1-[2-(indan-2-yl)ethyl]piperidin-4-yl]-1H-indole

https://huagongshe.com/reaction/275722

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-1-[1-[2-(indan-2-yl)ethyl]-1,2,3,6-tetrahydropyridin-4-yl]-1H-indoleHCID 18545836—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventAcetic AcidHCID 176—
Product5-Chloro-1-[1-[2-(indan-2-yl)ethyl]piperidin-4-yl]-1H-indoleHCID 18545841—

Reaction Steps

A mixture of 5-Chloro-1-[1-[2-(indan-2-yl)ethyl]-1,2,3,6-tetrahydropyridin-4yl]-1H-indol. 28a. (1.9 g), acetic acid (50 ml), and platinum oxide (0.1 g) was shaken for 3 h under 3 atm. hydrogen pressure. The mixture was filtered and evaporated in vacuo. The residue was dissolved in ethyl acetate and the organic phase was shaken with dilute ammonium hydroxide and then worked up in a conventional manner. Further purification was done on silica gel eluted with ethyl acetate-heptane (1:1) to give 2.0 g of crude product. The crude product was crystallized (ethyl acetate), and the title compound was collected by filtration (1.1 g, 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352988B2
Source datasetuspto-grants-2002_03
ORD IDord-54697a72aafd4e599ffd898a88433804
Source noteuspto-grants-2002_03