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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539785Generated: November 1, 2026

Acetic Acid → HCID 67983117, compound

https://huagongshe.com/reaction/539785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPyridineHCID 1049—
ReactantPivaloyl chlorideHCID 62493—
ReactantHCID 68089037HCID 68089037—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 67983117HCID 6798311744%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 6-(2-fluorophenyl)-2-(6-methyl-5-nitropyridin-3-yl)imidazo[1,2-b]pyridazine (0.016 g, 0.0458 mmol) in ethanol (3 mL) and water (1 mL) containing AcOH (0.274 mmol) is added iron (0.013 g, 0.229 mmol). The mixture is heated at 80° C. for 2 hours. The mixture is concentrated under reduced pressure and sat. aqueous NaHCO3 (10 mL) is added. The mixture is extracted with EtOAc (20 mL). Organic layer is collected and concentrated to dryness. Crude amine is taken up in acetonitrile (3 mL) containing pyridine (0.137 mmol). To this solution is added trimethylacetylchloride (0.0503 mmol). The mixture is stirred at room temperature for 4 hours, concentrated to dryness and then purified via silica chromatography using a gradient CH2Cl2 to CH2Cl2:EtOAc:methanol (1:1:0.1) to afford the title compound (0.008 g, 44%) as a light yellow solid: Rf 0.34 (1:1:0.1 CH2Cl2:EtOAc:methanol); LCMS (m/z)=404.4 [M+H]+, tR=2.11 min. (compound same as Example 390)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871767B2
Source datasetuspto-grants-2014_10
ORD IDord-64ab6fec4fff447c915b59735e5404c0
Source noteuspto-grants-2014_10