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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Acetyl-4-piperidone | HCID 122563 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 3-Amino-5-(pyridin-4-yl)thiophene-2-carboxamide | HCID 9920852 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 66743355 | HCID 66743355 | 52% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08691828B2 |
|---|
| Source dataset | uspto-grants-2014_04 |
|---|
| ORD ID | ord-3827b56836204ff1a62538c105404d56 |
|---|
| Source note | uspto-grants-2014_04 |
|---|