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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489475Generated: October 31, 2026

HCID 799039, compound → HCID 19082933, compound

https://huagongshe.com/reaction/1489475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 799039HCID 799039—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 19082933HCID 1908293382.6%

Reaction Steps

Ba) A solution of 42.5 g of N-(3-pyridinylmethyl)-benzamide in 220 ml of ethanol and 220 ml of 1N hydrochloric acid is treated with 4.2 g of palladium on charcoal and hydrogenated at room temperature for 24 hours over 100 bar of hydrogen. Then, the catalyst is filtered off and the filtrate is evaporated. The residue is taken up in methylene chloride and shaken with 1N sodium hydroxide solution. The organic phase is washed with water, dried and evaporated. There are obtained 36.1 g of (RS)-N-piperidin-3-ylmethyl-benzamide, MS (FAB): 218 M+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05677448
Source datasetuspto-grants-1997_10
ORD IDord-4a83d7307fc64072a2c9646ad9f860d8
Source noteuspto-grants-1997_10