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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972033Generated: October 30, 2026

Hydrochloric Acid → HCID 67387599, compound

https://huagongshe.com/reaction/1972033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantWaterHCID 962—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 67374614HCID 67374614—
CatalystAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
SolventWater ethylacetateHCID 22728543—
ProductHCID 67387599HCID 67387599166.1%

Reaction Steps

To a solution of 4-(4-benzyloxy-3-methoxy-phenyl)-3-butyl-6-(piperidin-4-yloxy)-pyridazine dihydrochloride (1.0 mmol, 520 mg) in dichloromethane (5.0 mL) was added formaldehyde solution in water (37%, 10 mmol, 1.0 mL), and 2 drops of acetic acid. Then sodium triacetoxyborohydride (4.0 mmol, 848 mg) was added. And the mixture was stirred at room temperature for 0.5 hour then condensed. It was then diluted with water/EtOAc and neutralized 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 (5.0 mL), 2N HCl in ether (5.0 mL) was added, kept at room temperature for 10 min, condensed, triturated with hexanes to afford 4-(4-benzyloxy-3-methoxy-phenyl)-3-butyl-6-(1-methyl-piperidin-4-yloxy)-pyridazine dihydrochloride (444 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431575B2
Source datasetuspto-grants-2013_04
ORD IDord-9ff5bac92bc4497fa27bbdcbd47d30c8
Source noteuspto-grants-2013_04