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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457817Generated: October 26, 2026

6-fluoro-3-(piperidin-4-yl)-1H-indole → 5-[4-(6-fluoro-1H-indol-3-yl)-piperidin-1-ylmethyl]2-methoxybenzoic acid ethyl ester

https://huagongshe.com/reaction/457817

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-fluoro-3-(piperidin-4-yl)-1H-indoleHCID 11096077—
Reactant5-Bromomethyl-2-methoxybenzoic acid ethyl esterHCID 68893946—
Product5-[4-(6-fluoro-1H-indol-3-yl)-piperidin-1-ylmethyl]2-methoxybenzoic acid ethyl esterHCID 68894051100.8%

Reaction Steps

This compound was prepared following the procedure described in example 1 (part D) starting with 0.5 g (2.2 mmol) of 6-fluoro-3-piperidin-4-yl-1H-indole and 0.8 g (2.9 mmol) of 5-bromomethyl-2-methoxy-benzoic acid ethyl ester. After standard purification, 0.91 g (100% of yield) of 5-[4-(6-fluoro-1H-indol-3-yl)-piperidin-1-ylmethyl]-2-methoxy-benzoic acid ethyl ester were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07189741B2
Source datasetuspto-grants-2007_03
ORD IDord-4efe466eb9294745b8a8879d9002a50b
Source noteuspto-grants-2007_03