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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362929Generated: October 30, 2026

HCID 54478803, compound → HCID 54111482, compound

https://huagongshe.com/reaction/362929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54478803HCID 54478803—
CatalystAdams' catalystHCID 345198—
SolventAcetic AcidHCID 176—
ProductHCID 54111482HCID 5411148283.8%

Reaction Conditions

Temperature40 °C

Reaction Steps

Step 1): A mixture of 2-(N'-n-heptylureido)-N-(pyridin-3-yl)benzamide obtained in the Example 34 (5.0 g, 14 mmol) and PtO2 in acetic acid (70 ml) was stirred at 40° C. under hydrogen atmosphere (50 psi) for 17 hours and then filtered. The filtrate was neutralized with 30% NaOH solution, extracted with ethyl acetate and washed with saturated NaHCO3 solution. The organic layer was dried (MgSO4) and concentrated. The residue was purified by column chromatography on silica gel (20% methanol and 0.8% NH4OH in dichloromethane) to give 2-(N'-n-heptylureido)-N-(piperidin-3-yl)benzamide (83.8%): mp 165° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05872115
Source datasetuspto-grants-1999_02
ORD IDord-20be24091fce4045926f430bb79d45da
Source noteuspto-grants-1999_02