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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517514Generated: October 31, 2026

4-Methoxybenzyl bromide → methyl (S)-2-(4-methanesulphonylpiperazin-1-yl)-3-[4-(4-methoxybenzyloxy)benzoylamino]propanoate

https://huagongshe.com/reaction/517514

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzyl bromideHCID 165021—
Reactantmethyl (S)-3-(4-hydroxybenzoylamino)-2-(4-methanesulphonylpiperazin-1-yl)propanoateHCID 67056914—
Productmethyl (S)-2-(4-methanesulphonylpiperazin-1-yl)-3-[4-(4-methoxybenzyloxy)benzoylamino]propanoateHCID 67057035100%

Reaction Steps

In a manner similar to example 4-5, starting from 300 mg (0.8 mmol) of methyl (S)-3-(4-hydroxybenzoylamino)-2-(4-methanesulphonylpiperazin-1-yl)propanoate (prepared as described in example 4-4) and from 0.14 ml (0.9 mmol) of 1-bromomethyl-4-methoxybenzene; 390 mg (100%) of methyl (S)-2-(4-methanesulphonylpiperazin-1-yl)-3-[4-(4-methoxybenzyloxy)benzoylamino]propanoate are obtained in the form of a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115102B2
Source datasetuspto-grants-2015_08
ORD IDord-47170daad6ad4f28b9bb28bba460ea3d
Source noteuspto-grants-2015_08