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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896280Generated: October 31, 2026

(Z)-ethyl 2-cyano-3-(4-(4-methylpiperazin-1-yl)phenyl)but-2-enoate → Methyl 2-cyano-3-(4-(4-methylpiperazin-1-yl)phenyl)butanoate

https://huagongshe.com/reaction/1896280

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Z)-ethyl 2-cyano-3-(4-(4-methylpiperazin-1-yl)phenyl)but-2-enoateHCID 86657557—
SolventMethanolHCID 887—
ProductMethyl 2-cyano-3-(4-(4-methylpiperazin-1-yl)phenyl)butanoateHCID 6738255057.7%

Reaction Steps

(Z)-ethyl 2-cyano-3-(4-(4-methylpiperazin-1-yl)phenyl)but-2-enoate (700 mg, 2.30 mmol) was added to a stirred mixture of Mg metal (2.10 g, 89.4 mmol) in methanol (20 ml) at 0° C. and stirred for 2 h at room temperature (reaction was activated by Mg metal, so exothermic). Then the reaction mixture was quenched with 6N HCl (20 ml) up to a clear solution was obtained. The reaction mixture was washed with ethyl acetate (2×20 ml), basified with saturated sodium bicarbonate and extracted with DCM (3×50 ml). The combined organic layer was washed with water, brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford 400 mg (54%) of methyl 2-cyano-3-(4-(4-methylpiperazin-1-yl)phenyl)butanoate as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518948B2
Source datasetuspto-grants-2013_08
ORD IDord-8b430566b297438e844256d7e5600306
Source noteuspto-grants-2013_08