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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220931Generated: October 30, 2026

Oxalyl chloride → 4-[2-(4-Cyclobutylmethyl-piperazin-1-yl)-2-oxo-ethyl]-3-methyl-benzoic Acid Methyl Ester

https://huagongshe.com/reaction/220931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(Cyclobutylmethyl)piperazine dihydrochlorideHCID 16801145—
Reactant2-(4-(Methoxycarbonyl)-2-methylphenyl)acetic acidHCID 57555224—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product4-[2-(4-Cyclobutylmethyl-piperazin-1-yl)-2-oxo-ethyl]-3-methyl-benzoic Acid Methyl EsterHCID 5755522546%

Reaction Steps

Oxalyl chloride (0.36 ml, 3.3 mmol) was added to a solution of 4-carboxymethyl-3-methyl-benzoic acid methyl ester from Example E32 (687 mg, 3.3 mmol) in dichloromethane (20 ml) and few drops of DMF. The mixture was stirred for 3 h at room temperature, concentrated in vacuo and azeotroped with toluene. The residue was dissolved in dichloromethane (10 ml) and added to a solution of 1-cyclobutylmethyl-piperazine dihydrochloride (750 mg, 3.3 mmol) in dichloromethane (10 ml) and DIEA (1.73 ml, 9.9 mmol) at 0° C. The mixture was stirred for 20 h at room temperature and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (eluant; 3% methanol:97% dichloromethane) to yield the title compound (528 mg, 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202858B2
Source datasetuspto-grants-2012_06
ORD IDord-bed5290ea06e499fbfbfec43c71cd610
Source noteuspto-grants-2012_06