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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426494Generated: November 1, 2026

Iodine → 4-Iodo-3-methoxy-6-pyridin-4-yl-pyridazine

https://huagongshe.com/reaction/2426494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
Reactant3-Methoxy-6-(pyridin-4-yl)pyridazineHCID 23092478—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-Iodo-3-methoxy-6-pyridin-4-yl-pyridazineHCID 2309246376.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

45 ml 1.6M solution of n-Butyllithium in hexane are added at −30° C. to a 10.2 g 2,2,6,6-tetramethylpiperidine in 100 ml THF, and the mixture is stirred at 0° C. for 30 min. After cooling to −75° C., 11.2 g 3-Methoxy-6-pyridin-4-yl-pyridazine dissolved 300 ml THF are added, and the solution is stirred at −75° C. for 35 min. The cold (−75° C.) reaction mixture is subsequently added to a cold (−75° C.) solution of 18.3 g iodine in 400 ml THF and stirred at −75° C. for 1.5 h. The reaction is quenched by adding 80 ml methanol/THF (1:1) at −75° C. and 300 ml saturated aqueous NaHCO3 at room temperature and extracted with dichloromethane. The organic layer is washed with 5% aqueous Na2S2O3 and saturated sodium chloride solution, dried (MgSO4) and the solvent removed. The crude product is purified by chromatography on silica gel to yield 14.4 g of 4-Iodo-3-methoxy-6-pyridin-4-yl-pyridazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968546B2
Source datasetuspto-grants-2011_06
ORD IDord-b9aca316e75c48e0908d67200d07303e
Source noteuspto-grants-2011_06