HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 2-[3-[4-[(4-Chlorophenyl)-2-pyridylmethoxy]-1-piperidyl]propylthio]benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-((4-Chlorophenyl)(4-piperidinyloxy)methyl)pyridine | HCID 11141197 | — |
| Reactant | 2-(3-Bromopropylthio)benzothiazole | HCID 14672135 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-[3-[4-[(4-Chlorophenyl)-2-pyridylmethoxy]-1-piperidyl]propylthio]benzothiazole | HCID 15055860 | 41% |
Reaction Steps
To a mixture of 0.76 g (2.51 mmol) of 4-[(4-chlorophenyl)-2-pyridylmethoxy]piperidine and 0.73 g (2.53 mmol) of 2-(3-bromopropylthio)benzothiazole, were added 6 ml of acetone and 0.35 g (2.53 mmol) of potassium carbonate, and the mixture was stirred at room temperature for 15 hours. After the reaction, the insolubles were filtered off, and the filtrate was concentrated under reduced pressure. The residue was separated by silica gel column chromatography using chloroform alone first, and then a mixture of chloroform and methanol in the volume ratio 30:1 as the eluent, and the desired fraction was concentrated to give 0.52 g (41%) of 2-[3-[4-[(4-chlorophenyl)-2-pyridylmethoxy]-1-piperidyl]propylthio]benzothiazole as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04929618 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-c5c007fb01f84ede8956fc10d5be29ae |
| Source note | uspto-grants-1990_05 |