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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363983Generated: October 31, 2026

N-Acetyl-4-piperidone → HCID 66743355, compound

https://huagongshe.com/reaction/2363983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Acetyl-4-piperidoneHCID 122563—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant3-Amino-5-(pyridin-4-yl)thiophene-2-carboxamideHCID 9920852—
SolventAcetic AcidHCID 176—
ProductHCID 66743355HCID 6674335552%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of 1-acetyl-4-piperidone (0.130 g, 0.920 mmol) and p-toluenesulfonic acid monohydrate (0.004 g, 0.02 mmol) in acetic acid (4 mL) was added 3-amino-5-(pyridin-4-yl)thiophene-2-carboxamide (0.050 g, 0.23 mmol). The mixture was heated at 80° C. for 5 h. Then, the reaction was allowed to cool to room temperature and concentrated. The obtained residue was dissolved in methanol (25 mL) and the solution was stirred with solid NaHCO3 (1.5 g) for 20 min. Then, the solution was filtered, and the filtrate was concentrated. The obtained residue was triturated with H2O. The obtained yellow solid was triturated with hot ethyl acetate to give the title compound (0.0407 g, 52%) as a yellow solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691828B2
Source datasetuspto-grants-2014_04
ORD IDord-3827b56836204ff1a62538c105404d56
Source noteuspto-grants-2014_04