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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646483Generated: October 31, 2026

Sodium Carbonate → ORG-13011 fumarate

https://huagongshe.com/reaction/1646483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantFumaric AcidHCID 444972—
Reactant1-[4-(Trifluoromethyl)pyridin-2-yl]piperazineHCID 11218492—
Reactant1-(4-Bromobutyl)pyrrolidin-2-oneHCID 15287841—
Solvent1-ButanolHCID 263—
SolventEthanolHCID 702—
ProductORG-13011 fumarateHCID 7068261552%

Reaction Steps

2 7 g of 1-(4-bromobutyl)-2-pyrrolidinone were mixed with 2.2 g of 1-[4-(trifluoromethyl)-2-pyridinyl]piperazine dissolved in 30 ml of butanol, after which 1.3 g of sodium carbonate were added. The mixture was refluxed for 2 hours, after which the precipitate was filtered and washed with butanol. The solvent was evaporated and the residue was dissolved in dichloromethane, washed with water, and dried over anhydrous magnesium sulfate. After evaporation of the solvent 3.4 g of 1-[4-[4-[4-(trifluoromethyl)-2-pyridinyl]-1-piperazinyl]butyl]-2-pyrrolidinone were obtained. To make the monofumarate, 1 g of fumaric acid dissolved in absolute ethanol was mixed with the free base. The resulting compound was recrystallized twice from acetonitrile, after which 2.4 g (52% yield) of 1-[4-[4-[4-(trifluoromethyl)-2-pyridinyl]-1-piperazinyl]butyl]-2pyrrolidinone (E)-2-butenedioate (1:1) salt were obtained with a melting point of 140° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180726
Source datasetuspto-grants-1993_01
ORD IDord-8b56b05798a44d2e966ff6125932fd2b
Source noteuspto-grants-1993_01