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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934581Generated: October 25, 2026

Water → (+/-)-ethyl alpha-ethyl-4,5-dihydro-4-[4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]-5-oxo-1H-1,2,4-triazol-1-acetate

https://huagongshe.com/reaction/1934581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
ReactantButanoic acid, 2-bromo-, ethyl esterHCID 79039—
Reactant2,4-Dihydro-4-(4-(4-(4-methoxyphenyl)piperazin-1-yl)phenyl)-3H-1,2,4-triazol-3-oneHCID 4246597—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product(+/-)-ethyl alpha-ethyl-4,5-dihydro-4-[4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]-5-oxo-1H-1,2,4-triazol-1-acetateHCID 8675804943%

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of 2,4-dihydro-4-[4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]-3H-1,2,4-triazol-3-one (0.05 mol), ethyl 2-bromobutanoate (0.055 mol) and Na2CO3 (0.15 mol) in 1-methyl-2-pyrrolidinone (250 ml) was stirred at 75° C. overnight. Ethyl 2-bromobutanoate (0.015 mol) was added again. The mixture was stirred at 75° C. for 6 hours, at room temperature for 48 hours, poured out into H2O and stirred for 30 minutes. The precipitate was filtered off and dissolved in CH2Cl2. The solution was filtered. The filtrate was dried, filtered and the solvent was evaporated. The residue was triturated in DIPE and ethyl acetate, filtered off and dried, yielding 10 g (43%) of (±)-ethyl α-ethyl-4,5-dihydro-4-[4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]-5-oxo-1H-1,2,4-triazol-1-acetate (interm. 9).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384030B1
Source datasetuspto-grants-2002_05
ORD IDord-98c8d9cf4a7b4e279a97bfbdcd5f6214
Source noteuspto-grants-2002_05