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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981635Generated: October 27, 2026

Thionyl Chloride → 3-[4-(2-Chloroethyl)-1-piperidinyl]-6-methylpyridazine

https://huagongshe.com/reaction/981635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-(1-(6-Methylpyridazin-3-YL)piperidin-4-YL)ethanolHCID 14989217—
SolventDichloromethaneHCID 6344—
Product3-[4-(2-Chloroethyl)-1-piperidinyl]-6-methylpyridazineHCID 14989218100%

Reaction Steps

To a stirred and cooled (ice bath) solution of 7.1 parts of thionyl chloride in 65 parts of dichloromethane was added dropwise a solution of 6.6 parts of 1-(6-methyl-3-pyridazinyl)-4-piperidineethanol in 195 parts of dichloromethane. Upon complete addition, stirring was continued overnight at room temperature. The reaction mixture was washed with alkaline water. The separated organic layer was dried, filtered and evaporated, yielding 7.2 parts (100%) of 3-[4-(2-chloroethyl)-1-piperidinyl]-6-methylpyridazine as a residue (int. 84).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04992433
Source datasetuspto-grants-1991_02
ORD IDord-ff29cab6af014747a6eab0ce0b5226a3
Source noteuspto-grants-1991_02