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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486474Generated: October 30, 2026

HCID 15124704, compound → HCID 178424721, compound

https://huagongshe.com/reaction/486474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15124704HCID 15124704—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Solvent2-MethoxyethanolHCID 8019—
ProductHCID 178424721HCID 17842472197%

Reaction Steps

A mixture of 6.1 parts of 4-(3-methylphenyl)-1-[6-(phenylmethoxy)-3-pyridazinyl]-4-piperidinol and 250 parts of 2-methoxyethanol was hydrogenated at normal pressure and at room temperature with 2 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The residue was boiled in 2-propanol. The product was filtered off and dried, yielding 4.5 parts (97%) of 6-[4-hydroxy-4-(3-methylphenyl)-1-piperidinyl)-3-pyridazinol; mp. 264.6° C. (compound 269).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292738
Source datasetuspto-grants-1994_03
ORD IDord-722a0f42a0014d3f95cc03317e1b6be4
Source noteuspto-grants-1994_03