HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984151Generated: October 29, 2026
Potassium Iodide → HCID 22557840, compound
https://huagongshe.com/reaction/984151
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Chloromethyl-2-(3,4,5-trimethoxyphenyl) pyridine | HCID 12019237 | — |
| Reactant | HCID 12043124 | HCID 12043124 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22557840 | HCID 22557840 | — |
Reaction Steps
4-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyloxy]piperidine (70 mg), 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (22 mg), potassium carbonate (56 mg) and potassium iodide (40 mg) were suspended in acetonitrile (5 mL). The mixture was stirred at room temperature for 5 hr and evaporated. Chloroform and water were added to the residual oil and the organic layer was separated. Aqueous layer was then extracted with chloroform and the organic layers were combined, dried over anhydrous magnesium sulfate and evaporated. The residue was applied to a column of silica gel using chloroform-methanol (40:1) as an eluent. Fractions containing the product were collected and evaporated. The title compound was obtained by converting the free base to a trihydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06867221B2 |
|---|
| Source dataset | uspto-grants-2005_03 |
|---|
| ORD ID | ord-e2fd8f284288437ca904b772bcad1aac |
|---|
| Source note | uspto-grants-2005_03 |
|---|