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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253598Generated: October 26, 2026

Sodium Hydroxide → 6-Chloro-2-phenyl-3-(pyridazin-4-yl)imidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/1253598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactanto-ChloranilHCID 73252—
ReactantEthyl 4-[6-chloro-2-phenylimidazo[1,2-b]pyridazin-3-yl]-4H-pyridazine-1-carboxylateHCID 59367705—
SolventChloroformHCID 6212—
Product6-Chloro-2-phenyl-3-(pyridazin-4-yl)imidazo[1,2-b]pyridazineHCID 5936770471.2%

Reaction Steps

22.3 g (58.4 mmol) of ethyl 4-[6-chloro-2-phenylimidazo[1,2-b]pyridazin-3-yl]-4H-pyridazine-1-carboxylate are dissolved in 450 ml of chloroform and 15.1 g (61.3 mmol) of ortho-chloranil are added portionwise. The reaction medium is stirred for 30 minutes at ambient temperature and then poured into a 2N aqueous solution of sodium hydroxide. The product is extracted with chloroform. The organic phase is dried over sodium sulfate and then concentrated under reduced pressure. The dark beige residue is crystallized from a mixture of 80 ml of isopropanol and 60 ml of diisopropyl ether under hot conditions, to give 12.8 g of a beige powder after cooling, isolation by filtration and drying.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455491B2
Source datasetuspto-grants-2013_06
ORD IDord-e4c597aa6b224362b9e51ac89fb85208
Source noteuspto-grants-2013_06