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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325922Generated: October 29, 2026

HCID 20262412, compound → HCID 20262416, compound

https://huagongshe.com/reaction/325922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20262412HCID 20262412—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventDimethylacetamideHCID 31374—
ProductHCID 20262416HCID 20262416—

Reaction Steps

A mixture of 65 parts of 1-benzoyl-4-(5-fluoro-1H-indol-3-yl)-1,4-dihydropyridine and 270 parts of N,N-dimethylacetamide was hydrogenated at normal pressure and at room temperature with 10 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 poured onto water and the product was extracted with 4-methyl-2-pentanone. The extract was dried, filtered and evaporated. The residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 5 parts of 1-benzoyl-4-(5-fluoro-1H-indol-3-yl)piperidine as a residue (intermediate 21).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04443451
Source datasetuspto-grants-1984_04
ORD IDord-834b76ed6f5041d68d15dace7defb452
Source noteuspto-grants-1984_04