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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846782Generated: October 30, 2026

HCID 15096761, compound → HCID 67914605, compound

https://huagongshe.com/reaction/846782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15096761HCID 15096761—
ReactantHCID 178418361HCID 178418361—
SolventAcetic AcidHCID 176—
ProductHCID 67914605HCID 67914605—

Reaction Steps

A mixture of 9 parts of cis-1-(1H-benzimidazol-2-ylmethyl)-3-methoxy-4-piperidinamine and 150 parts of acetic acid was hydrogenated at normal pressure and at room temperature with 2 parts of rhodium-on-charcoal catalyst 5%. 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 (90:10 by volume) saturated with ammonia, as eluent. The second fraction was collected and the eluent was evaporated, yielding 5 parts of cis-3-methoxy-1-[(4,5,6,7-tetrahydro-1H-benzimidazol-2-yl)-methyl]-4-piperidinamine as a residue (intermediate 113).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05137896
Source datasetuspto-grants-1992_08
ORD IDord-0b94038323a24772a183710b6c3279aa
Source noteuspto-grants-1992_08