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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270456Generated: November 2, 2026

Sodium hydride → 3-[(6-(Imidazol-1-yl)pyridazin-3-yl)oxy]-1-benzylpiperidine

https://huagongshe.com/reaction/1270456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3-Chloro-6-(1H-imidazol-1-yl)pyridazineHCID 2770903—
Reactant1-Benzyl-3-piperidinol hydrochlorideHCID 16218306—
SolventDimethylformamideHCID 6228—
Product3-[(6-(Imidazol-1-yl)pyridazin-3-yl)oxy]-1-benzylpiperidineHCID 2226006436.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202263B2
Source datasetuspto-grants-2007_04
ORD IDord-c4418328a60f4673aba7813a4b275abf
Source noteuspto-grants-2007_04