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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457802Generated: October 29, 2026

Methyl 3-(bromomethyl)benzoate → 3-[4-(1H-indol-3-yl)-piperidin-1-ylmethyl]-benzoic acid methyl ester

https://huagongshe.com/reaction/457802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-(bromomethyl)benzoateHCID 517981—
Reactant3-(4-Piperidinyl)-1H-indoleHCID 702235—
Product3-[4-(1H-indol-3-yl)-piperidin-1-ylmethyl]-benzoic acid methyl esterHCID 6941236979.2%

Reaction Steps

This compound was prepared following the procedure described in example 1 (part D) starting with 0.2 g (1 mmol) of 3-piperidin-4-yl-1H-indole and 0.29 g (1.3 mmol) of 3-bromomethyl-benzoic acid methyl ester. After ionic exchange purification, 0.276 g (79% of yield) of 3-[4-(1H-indol-3-yl)-piperidin-1-ylmethyl]-benzoic acid methyl ester were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07189741B2
Source datasetuspto-grants-2007_03
ORD IDord-bc65c44d450f445f9cf7d89f28fd08e4
Source noteuspto-grants-2007_03