HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 3-[(6-(Imidazol-1-yl)pyridazin-3-yl)oxy]-1-benzylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Chloro-6-(1H-imidazol-1-yl)pyridazine | HCID 2770903 | — |
| Reactant | 1-Benzyl-3-piperidinol hydrochloride | HCID 16218306 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[(6-(Imidazol-1-yl)pyridazin-3-yl)oxy]-1-benzylpiperidine | HCID 22260064 | 36.1% |
Reaction Steps
To a suspension of NaH (0.21 g, 8.31 mmol) in DMF (5 mL) was added 1-benzyl-3-hydroxypiperidine hydrochloride (0.78 g, 3.3 mmol) in DMF (5 mL), and the resulting reaction mixture was stirred at ambient temperature for 30 minutes. 3-chloro-6-(imidazol-1-yl)pyridazine (0.6 g, 3.3 mmol) in DMF (5 mL) was then added dropwise. The reaction mixture was stirred at ambient temperature for 30 minutes. After removal of DMF in vacuo, the black oil was dissolved in CH2Cl2 (50 mL), washed with water and brine. Purification using column chromatography afforded 3-[(6-(imidazol-1-yl)pyridazin-3-yl)oxy]-1-benzylpiperidine (400 mg) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06982259B2 |
| Source dataset | uspto-grants-2006_01 |
| ORD ID | ord-b96741ec8f0b499787ca3a2ad84a2a5c |
| Source note | uspto-grants-2006_01 |