HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275281Generated: October 30, 2026
1-{4-[1-(2-Phenylethyl)-1H-imidazole-2-carbonyl]piperidin-1-yl}ethan-1-one → HCID 19371531, compound
https://huagongshe.com/reaction/275281
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-{4-[1-(2-Phenylethyl)-1H-imidazole-2-carbonyl]piperidin-1-yl}ethan-1-one | HCID 20087754 | — |
| Reactant | HCID 20087755 | HCID 20087755 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 19371531 | HCID 19371531 | 27% |
Reaction Steps
A mixture (3.87 g) of 1-acetyl-4-[[1-(2-phenylethyl)-1H-imidazol-2yl]carbonyl]piperidine (D), (1-acetyl-4-pipendinylidene)[1-(2-phenylethyl)-1H-imidazol-2-yl]methyl 1 -acetyl-4-piperidine carboxylate (H), and 6 N hydrochloric acid (100 ml) was refluxed for 20 hrs. The cooled reaction mixture was concentrated, and the residue was diluted with water. The resulting mixture was sequentially washed with ether and ethyl acetate. The acidic aqueous layer was basified with sodium hydroxide solution and was extracted with dichloromethane. The combined extracts were washed with water, dried, filtered, and concentrated to give [1-(2-phenyethyl)-1H-imidazol-2-yl](4-piperidinyl) methanone (K, 0.91 g), m.p. 230°-232° C. from dichloromethane-hexanes. ##STR31##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05393753 |
|---|
| Source dataset | uspto-grants-1995_02 |
|---|
| ORD ID | ord-21aec81edd764800914f541bc73dc18d |
|---|
| Source note | uspto-grants-1995_02 |
|---|