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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402929Generated: October 25, 2026

Sodium hydride → [6-(6-Chloro-imidazo[1,2-b]pyridazin-8-ylamino)-pyridin-3-yl]-morpholin-4-yl-methanone

https://huagongshe.com/reaction/402929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant8-Bromo-6-chloroimidazo(1,2-b)pyridazineHCID 46835269—
Reactant(6-Aminopyridin-3-yl)(morpholino)methanoneHCID 59259223—
SolventDimethylformamideHCID 6228—
Product[6-(6-Chloro-imidazo[1,2-b]pyridazin-8-ylamino)-pyridin-3-yl]-morpholin-4-yl-methanoneHCID 57786785100.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 8-bromo-6-chloroimidazo[1,2-b]pyridazine (272 mg, 1.17 mmol, Eq: 1.00) and (6-aminopyridin-3-yl)(morpholino)methanone (255 mg, 1.23 mmol, Eq: 1.05) in DMF (10.0 ml) was cooled to 0° C. To this reaction mixture was added sodium hydride (150 mg, (60% in mineral oil), 3.74 mmol, Eq: 3.2). The reaction was allowed to stir at 0° C. for 10 minutes and then allowed to warm to room temperature and stir 18 h. The reaction mixture was quenched with sat. NaHCO3 (aq) and diluted with water and EtOAc. An insoluble solid was collected by filtration to give [6-(6-chloro-imidazo[1,2-b]pyridazin-8-ylamino)-pyridin-3-yl]-morpholin-4-yl-methanone (420 mg, 99%). LC/MS-ESI observed [M+H]+ 358.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742098B2
Source datasetuspto-grants-2014_06
ORD IDord-d3dbf29455954ae3a7d53f501695c330
Source noteuspto-grants-2014_06