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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981650Generated: October 30, 2026

Sodium Carbonate → Ethyl 4-[2-[1-(6-butyl-3-pyridazinyl)-4-piperidinyl]ethoxy]benzoate

https://huagongshe.com/reaction/981650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantEthyl 4-[2-(4-piperidinyl)ethoxy]benzoateHCID 14989200—
Reactant3-Butyl-6-chloropyridazineHCID 14989301—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-[2-[1-(6-butyl-3-pyridazinyl)-4-piperidinyl]ethoxy]benzoateHCID 1498930820.8%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 2.4 parts of 3-butyl-6-chloropyridazine, 4.2 parts of ethyl 4-[2-(4-piperidinyl)ethoxy]benzoate and 2.1 parts of sodium carbonate was stirred for 4 hours at 140° C. After cooling, the reaction mixture was taken up in water and dichloromethane. The separated organic layer was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (98:2 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 2,2'-oxybispropane. The product was filtered off, washed with 2,2'-oxybispropane and dried at 50° C., yielding 1.2 parts (20.8%) of ethyl 4-[2-[1-(6-butyl-3-pyridazinyl)-4-piperidinyl]ethoxy]benzoate; mp. 91.4° C. (comp. 84).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04992433
Source datasetuspto-grants-1991_02
ORD IDord-76928e7bd9144790a749623dde1584a9
Source noteuspto-grants-1991_02