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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251847Generated: November 1, 2026

HCID 69088302, compound → HCID 69032357, compound

https://huagongshe.com/reaction/2251847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69088302HCID 69088302—
SolventEthanolHCID 702—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 69032357HCID 69032357—

Reaction Steps

N-(5-Nitro-2-tert-butylpheny)-2-piperidin-1-yl-acetamide (1.77 g, 5.5 mmol) was dissolved in EtOH (100 mL) and 1,4-dioxane (10 mL). The solution was degassed under vacuum with stirring. A catalytic amount of 5% Pd/C was added (as a slurry in EtOH). The mixture was degassed again, then the reaction vessel was charged with H2 gas (balloon) and stirred overnight at RT. The reaction was filtered through Celite® with MeOH and the filtrate was concentrated under reduced pressure. The recovered material was eluted through a column of silica gel with a 5 to 40% (90:10:1 CH2Cl2:MeOH:NH4OH(aq)) to CH2Cl2 linear gradient giving a brown foamy solid. MS: 290 (M+1). Calc'd. for C17H27N3O—289.42.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07320992B2
Source datasetuspto-grants-2008_01
ORD IDord-4d68cc192b834a6bb0c75c64d39cc6e3
Source noteuspto-grants-2008_01