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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874593Generated: October 29, 2026

4-(2-Methylquinolin-4-ylmethoxy)benzenesulfonyl chloride hydrochloride → Methyl (S)-2-[4-(2-methylpropene-1-sulfonyl)piperazin-1-yl]-3-(4-(2-methylquinolin-4-ylmethoxy)benzenesulfonylamino)propanoate

https://huagongshe.com/reaction/874593

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Methylquinolin-4-ylmethoxy)benzenesulfonyl chloride hydrochlorideHCID 86607865—
Reactantmethyl (S)-3-amino-2-[4-(2-methylpropane-1-sulfonyl)piperazin-1-yl]propanoate dihydrochlorideHCID 86715684—
Reactantmethyl (S)-2-[4-(2-methylpropane-1-sulfonyl)piperazin-1-yl]-3-[4-(2-methylquinolin-4-ylmethoxy)benzenesulfonylamino]propanoateHCID 86715687—
ProductMethyl (S)-2-[4-(2-methylpropene-1-sulfonyl)piperazin-1-yl]-3-(4-(2-methylquinolin-4-ylmethoxy)benzenesulfonylamino)propanoateHCID 86715686—

Reaction Steps

In a manner analogous to example 3.6, using 621 mg (1.6 mmol) of methyl (S)-3-amino-2-[4-(2-methylpropane-1-sulfonyl)piperazin-1-yl]propanoate dihydrochloride and 876 mg (2.3 mmol) of 4-(2-methylquinolin-4-ylmethoxy)benzenesulfonyl chloride hydrochloride (prepared as described in example 17.2), 643 mg (64%) of methyl (S)-2-[4-(2-methylpropane-1-sulfonyl)piperazin-1-yl]-3-[4-(2-methylquinolin-4-ylmethoxy)benzenesulfonylamino]propanoate are obtained in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980897B2
Source datasetuspto-grants-2015_03
ORD IDord-9f5ab65d5fb2404a9afbc2d9ffcc5c53
Source noteuspto-grants-2015_03