Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030916Generated: October 26, 2026

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

https://huagongshe.com/reaction/1030916

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 numberUS05106973
Source datasetuspto-grants-1992_04
ORD IDord-7b0982b4f4ef49559c0401f5edd43096
Source noteuspto-grants-1992_04