Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | HCID 67067457 | HCID 67067457 | — |
| Reactant | Sodium bicarbonate water | HCID 86585896 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 178489883 | HCID 178489883 | 31.7% |
Reaction Steps
A solution of (E)-N-[3-(4-fluorophenyl)-2-oxopropyl]-3-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]acrylamide (43 mg) and ammonium acetate (163 mg) in acetic acid (1 mL) and xylene (5 mL) was heated under reflux for 16 hours. The reaction solution was left to cool to room temperature. Ethyl acetate and saturated sodium bicarbonate water were added to the reaction solution, and the organic layer was separated. The resulting organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (carrier: Chromatorex™ NH; elution solvent: ethyl acetate→ethyl acetate:methanol=5:1) to obtain 13 mg of the title compound. The property values of the compound are as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07897632B2 |
|---|
| Source dataset | uspto-grants-2011_03 |
|---|
| ORD ID | ord-9882cb93c2434ff893dda354da80195f |
|---|
| Source note | uspto-grants-2011_03 |
|---|