HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 3-[4-(2-Chloroethyl)-1-piperidinyl]-6-methylpyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-(1-(6-Methylpyridazin-3-YL)piperidin-4-YL)ethanol | HCID 14989217 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[4-(2-Chloroethyl)-1-piperidinyl]-6-methylpyridazine | HCID 14989218 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05106973 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-7b0982b4f4ef49559c0401f5edd43096 |
| Source note | uspto-grants-1992_04 |