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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517512Generated: October 31, 2026

1-(Bromomethyl)naphthalene → Methyl (S)-2-(4-methanesulphonylpiperazin-1-yl)-3-[4-(naphthalen-1-ylmethoxy)benzoylamino]propanoate

https://huagongshe.com/reaction/517512

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Bromomethyl)naphthaleneHCID 137844—
Reactantmethyl (S)-3-(4-hydroxybenzoylamino)-2-(4-methanesulphonylpiperazin-1-yl)propanoateHCID 67056914—
Reactantmethyl (S)-2-(4-methanesulphonylpiperazin-1-yl)-3-[4-(2-methylquinolin-4-ylmethoxy)benzoylamino]-propanoateHCID 86667909—
ProductMethyl (S)-2-(4-methanesulphonylpiperazin-1-yl)-3-[4-(naphthalen-1-ylmethoxy)benzoylamino]propanoateHCID 86667908—

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 200 mg (1.2 mmol) of 1-bromomethylnaphthalene, 320 mg (78%) of methyl (S)-2-(4-methanesulphonylpiperazin-1-yl)-3-[4-(2-methylquinolin-4-ylmethoxy)benzoylamino]-propanoate are obtained in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115102B2
Source datasetuspto-grants-2015_08
ORD IDord-41dcbb00c1ac4f79b59412b095c5e65e
Source noteuspto-grants-2015_08