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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309621Generated: October 25, 2026

1-benzoyl-1,4-dihydro-4-[(1-methyl-1H-benzimidazol-2-yl)methyl]pyridine → 1-benzoyl-4-[(1-methyl-1H-benzimidazol-2-yl)methyl]pyridine

https://huagongshe.com/reaction/2309621

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-benzoyl-1,4-dihydro-4-[(1-methyl-1H-benzimidazol-2-yl)methyl]pyridineHCID 14518094—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product1-benzoyl-4-[(1-methyl-1H-benzimidazol-2-yl)methyl]pyridineHCID 2003790658.5%

Reaction Steps

A mixture of 16 parts of 1-benzoyl-1,4-dihydro-4-[(1-methyl-1H-benzimidazol-2-yl)methyl]pyridine and 160 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. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (97.5:2.5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The oily residue was crystallized from 14 parts of 1,1'-oxybisethane. The product was filtered off and dried, yielding 7.8 parts (58.5%) of 1-benzoyl-4-[(1-methyl-1H-benzimidazol-2-yl)methyl]pyridine; mp. 159.3° C. (32).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04695575
Source datasetuspto-grants-1987_09
ORD IDord-bdcc0d70fc3941dab7307dc48682ebaa
Source noteuspto-grants-1987_09