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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1924273Generated: November 2, 2026

HCID 17948959, compound → HCID 15953078, compound

https://huagongshe.com/reaction/1924273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 17948959HCID 17948959—
Reactant(6-Chloro-2-cyclopropylimidazo[1,2-b]pyridazin-3-yl)methanolHCID 58009731—
SolventTolueneHCID 1140—
ProductHCID 15953078HCID 1595307828%

Reaction Steps

A solution of (6-chloro-2-cyclopropylimidazo[1,2-b]pyridazin-3-yl)methanol x115 (889 mg, 3.97 mmol), 4-(2,2-difluorovinyl)pyrrolidin-2-one (643 mg, 4.37 mmol, 1.1 eq) and paratoluenesulfonic acid (76 mg, 0.40 mmol, 0.1 eq) in toluene (20 ml) is heated under reflux for 16 h. After cooling, the solvent is removed under reduced pressure, the crude product is dissolved in dichloromethane (100 ml). The organic layer is washed by water (150 ml). The aqueous layer is extracted by dichloromethane (100 ml). The cumulated organic layers are dried over MgSO4, filtered and evaporated under reduced pressure. The residue is purified by preparative chromatography over silicagel (benzine/AcOEt:60/40) to afford 1-[(6-chloro-2-cyclopropylimidazo[1,2-b]pyridazin-3-yl)methyl]-4-(2,2-difluorovinyl)pyrrolidin-2-one 62 after recrystallization in diisopropylether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178533B2
Source datasetuspto-grants-2012_05
ORD IDord-bd5f252e7c634ea086c29a1721c37ec5
Source noteuspto-grants-2012_05