HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Pyridin-4-yl)malonaldehyde → (S)-N-((3-(3-fluoro-4-(4-(pyridin-4-yl)-1H-pyrazol-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Pyridin-4-yl)malonaldehyde | HCID 2737246 | — |
| Reactant | (S)-N-((3-(3-fluoro-4-hydrazinophenyl)-2-oxooxazolidin-5-yl)methyl)acetamide | HCID 10731576 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (S)-N-((3-(3-fluoro-4-(4-(pyridin-4-yl)-1H-pyrazol-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide | HCID 71477480 | 66.3% |
Reaction Steps
100 mg (0.354 mmol) of (S)—N-{[3-(3-fluoro-4-hydrazinophenyl)-2-oxooxazolidin-5-yl]methyl}-acetamide and 52.8 mg (0.354 mmol) of 2-(4-pyridyl)malondialdehyde were combined with 5 mL ethanol as a solvent. Then, the resultant mixture was slowly heated to reflux, thereby the solid was substantially dissolved. TLC monitoring was performed to determine completion of the reaction. Then, the resultant mixture was cooled to room temperature and vacuum filtered to afford the product (13a) as a light yellow solid, with a yield of 66.3%, melting point: 203.8-205.0° C., HPLC: 99.97%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08946436B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-e84dd3d7177f4e37a0b4eaa0b82da4ba |
| Source note | uspto-grants-2015_02 |