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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457827Generated: November 4, 2026

Ethyl 4-(1H-indol-3-yl)piperidine-1-carboxylate → HCID 69413356, compound

https://huagongshe.com/reaction/457827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-(1H-indol-3-yl)piperidine-1-carboxylateHCID 11380267—
ReactantHCID 21414365HCID 21414365—
ProductHCID 69413356HCID 6941335660.1%

Reaction Steps

This compound was prepared following the procedure described in example 13 (part B) starting with 11 g (40 mmol) of 4-(1H-indol-3-yl)-piperidine-1-carboxylic acid ethyl ester and 9.6 g (48 mmol) of 5-(2-chloro-ethoxy)-benzo[1,3]dioxole. The mixture was stirred at room temperature for 18 hours. After standard work-up and purification, 10.5 g (60% of yield) of 4-{1-[2-(benzo[1,3]dioxol-5-yloxy)-ethyl]-1H-indol-3-yl}-piperidine-1-carboxylic acid ethyl ester were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07189741B2
Source datasetuspto-grants-2007_03
ORD IDord-f73808fa91f04c9c90fd9408fae933b1
Source noteuspto-grants-2007_03