HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605796Generated: October 31, 2026
6-Chloro-2-picoline → HCID 57507761, compound
https://huagongshe.com/reaction/605796
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-Chloro-2-picoline | HCID 87601 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 57421831 | HCID 57421831 | — |
| Catalyst | 2-(Dicyclohexylphosphino)biphenyl | HCID 2734216 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57507761 | HCID 57507761 | 91.4% |
Reaction Steps
In an argon atmosphere, sodium tert-butoxide, (0.52 g), tris(dibenzylideneacetone)dipalladium (100 mg) and 2-(dicyclohexylphosphino)biphenyl (76 mg) were added to a Tol (22 ml) solution of 2-chloro-6-methylpyridine (0.56 g) and tert-butyl 4-[3-(4-piperidinyl)propyl]-1-piperidinecarboxylate (1.1 g), followed by heating with stirring at 100° C. for 1 hour. This was cooled to room temperature, diluted with EtOAc, and washed with aqueous saturated sodium hydrogencarbonate solution. This was dried over anhydrous magnesium sulfate, the solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (eluent: hexane:EtOAc=10:1 (v/v)) to obtain tert-butyl 4-{3-[1-(6-methyl-2-pyridinyl)-4-piperidyl]propyl}-1-piperidinecarboxylate (1.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07915261B2 |
|---|
| Source dataset | uspto-grants-2011_03 |
|---|
| ORD ID | ord-457187bb4e8a423a855019c5f187b403 |
|---|
| Source note | uspto-grants-2011_03 |
|---|