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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097314Generated: November 1, 2026

Sodium Iodide → 4-imidazo[1,2-b]pyridazin-7-yl-1-(3-piperidin-1-yl-propyl)-1H-pyridin-2-one

https://huagongshe.com/reaction/1097314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantN-(3-chloropropyl)piperidine hydrochlorideHCID 79624—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178515730HCID 178515730—
SolventDimethylformamideHCID 6228—
Product4-imidazo[1,2-b]pyridazin-7-yl-1-(3-piperidin-1-yl-propyl)-1H-pyridin-2-oneHCID 59443509—

Reaction Conditions

Temperature60 °C

Reaction Steps

4-Imidazo[1,2-b]pyridazin-7-yl-pyridin-2-ol (1 eq, 0.17 mmol, 36 mg), 1-(3-chloropropyl)piperidine monohydrochloride (1.5 eq, 0.255 mmol, 52 mg) and sodium iodide (1.5 eq, 0.254 mmol, 37.9 mg) are dissolved in DMF (1 ml) and heated at 60° C. for 16 h to give a black solution. The reaction mixture is then poured into aq. sat. NaHCO3 and the organic phase is extracted with CH2Cl2. The organic phase is washed with brine, dried over MgSO4, filtered and evaporated to dryness to afford 4-imidazo[1,2-b]pyridazin-7-yl-1-(3-piperidin-1-yl-propyl)-1H-pyridin-2-one; [M+H]+=338

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143253B2
Source datasetuspto-grants-2012_03
ORD IDord-a2b49cd9be2a42cbbede1bc38ca88ac7
Source noteuspto-grants-2012_03