Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904826Generated: November 2, 2026

3-[(4-methoxyphenyl)methyl]-2-[[1-(phenylmethyl)-4-piperidinyl]methyl]-3H-imidazo[4,5-b]-pyridine → 3-[(4-methoxyphenyl)methyl]-2-(4-piperidinylmethyl)-3H-imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/1904826

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[(4-methoxyphenyl)methyl]-2-[[1-(phenylmethyl)-4-piperidinyl]methyl]-3H-imidazo[4,5-b]-pyridineHCID 14013369—
ReactantHCID 14518103HCID 14518103—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-[(4-methoxyphenyl)methyl]-2-(4-piperidinylmethyl)-3H-imidazo[4,5-b]pyridineHCID 1451800989%

Reaction Steps

A mixture of 41 parts of 3-[(4-methoxyphenyl)methyl]-2-[[1-(phenylmethyl)-4-piperidinyl]methyl]-3H-imidazo[4,5-b]-pyridine and 480 parts of methanol was hydrogenated at normal pressure and at 50° C. with 5 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, yielding 30 parts (89%) of 3-[(4-methoxyphenyl)methyl]-2-(4-piperidinylmethyl)-3H-imidazo[4,5-b]pyridine (37). In a similar manner there were also prepared:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04839374
Source datasetuspto-grants-1989_06
ORD IDord-0eb631fae0274aab8797c6595a6ede7e
Source noteuspto-grants-1989_06