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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981657Generated: October 31, 2026

Sodium Iodide → HCID 14989359, compound

https://huagongshe.com/reaction/981657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-4-methoxyphenolHCID 87459—
ReactantHCID 14989321HCID 14989321—
SolventAcetonitrileHCID 6342—
ProductHCID 14989359HCID 1498935941.3%

Reaction Steps

To a stirred solution of 3.0 parts of 3-chloro-6-[4-(3-chloropropyl)-1-piperidinyl]-pyridazine in 80 parts of acetonitrile were added 2.1 parts of sodium iodide. The reaction mixture was stirred for 2 hours at reflux temperature. After cooling, a mixture of 2.2 parts of 2-chloro-4-methoxyphenol and 3.8 parts of potassium carbonate was added to the mixture and the whole was stirred for 2 days at reflux temperature. The reaction mixture was evaporated and the residue was taken up in water. The product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (99:1 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 2-propanol. The product was filtered off and dried at 70° C., yielding 1.8 parts (41.3%) of 3-chloro-6-[4-[3-(2-chloro-4-methoxyphenoxy)propyl]-1-piperidinyl]pyridazine; mp. 101.0° C. (comp. 141).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04992433
Source datasetuspto-grants-1991_02
ORD IDord-40547017d7574d139ad3f72da43feca8
Source noteuspto-grants-1991_02