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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457791Generated: October 25, 2026

2-(Bromomethyl)furan → 4-(6-fluoro-1-furan-2-ylmethyl-1H-indol-3-yl)-piperidine-1-carboxylic acid ethyl ester

https://huagongshe.com/reaction/457791

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Bromomethyl)furanHCID 4603765—
Reactant4-(6-fluoro-1H-indol-3-yl)-piperidine-1-carboxylic acid ethyl esterHCID 11323738—
Product4-(6-fluoro-1-furan-2-ylmethyl-1H-indol-3-yl)-piperidine-1-carboxylic acid ethyl esterHCID 11349225100.5%

Reaction Steps

This compound was obtained following procedure described in example 13 (part B) at room temperature for 5 hours, starting with 5 g (17.2 mmol) of 4-(6-fluoro-1H-indol-3-yl)-piperidine-1-carboxylic acid ethyl ester were and 3.2 g (20 mmol) of 2-bromomethyl-furan. After standard work-up, 6.4 g (99% of yield) of 4-(6-fluoro-1-furan-2-ylmethyl-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-b6b8cf0fc646427497229658acfff45a
Source noteuspto-grants-2007_03