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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362926Generated: October 31, 2026

HCID 53904510, compound → HCID 53783949, compound

https://huagongshe.com/reaction/362926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 53904510HCID 53904510—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 53783949HCID 53783949—

Reaction Steps

Step 1): 10% Pd/C was added to a solution of the N-(1-benzylpiperidin-4yl)-2-(N'-n-heptylureido)benzamide (1.4 g, 3.1 mmol) obtained in Example 41 in methanol (25 ml) under nitrogen. The mixture was shaken under 50 psi hydrogen pressure for 5 hours, and then filtered under nitrogen. The filtrate was concentrated. The residue was purified by column chromatography on silica gel (50% methanol and 0.8% NH4OH in dichloromethane) to give N-(piperidin-4-yl)-2-(N'-n-heptylureido)benzamide: 48.4%: mp 159° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05872115
Source datasetuspto-grants-1999_02
ORD IDord-990a66254f79419396dbf2bb2d2e2fed
Source noteuspto-grants-1999_02