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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168723Generated: October 31, 2026

Hydrochloric Acid → HCID 67374073, compound

https://huagongshe.com/reaction/2168723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 67371453HCID 67371453—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
SolventWater ethylacetateHCID 22728543—
ProductHCID 67374073HCID 67374073—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 3-butyl-4-(4-cyclohexyloxy-3-nitro-phenyl)-6-(1-methyl-piperidin-4-yloxy)-pyridazine (5 mmol, 2.34 g) in acetic acid (10 mL) was added iron powder (˜325 mesh, 50 mmol, 2.80 g). And the mixture was stirred at 100° C. for 0.5 hour. It was then diluted with water/EtOAc and neutralized slowly with NaHCO3 powder. The solvent was removed in vacuo and the residue was purified by silica gel chromatography (DCM to DCM+10% 2N NH3 in MeOH) to give a colorless sticky solid, which was dissolved in DCM (10 mL), 2N HCl in ether (10 mL) was added, kept at room temperature for 10 min, condensed, triturated with hexanes to provide 5-[3-butyl-6-(1-methyl-piperidin-4-yloxy)-pyridazin-4-yl]-2-cyclohexyloxy-phenylamine trihydrochloride (2.06 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045461B2
Source datasetuspto-grants-2015_06
ORD IDord-f7471132fd6f4d23ab1598025802b3d3
Source noteuspto-grants-2015_06