HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxo[3-(2-oxopyrrolidin-1-yl)phenyl]acetaldehyde → 1-{3-[3-(2,4-Difluorophenyl)-[1,2,4]triazin-5-yl]phenyl}pyrrolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxo[3-(2-oxopyrrolidin-1-yl)phenyl]acetaldehyde | HCID 22273606 | — |
| Reactant | HCID 178506601 | HCID 178506601 | — |
| Product | 1-{3-[3-(2,4-Difluorophenyl)-[1,2,4]triazin-5-yl]phenyl}pyrrolidin-2-one | HCID 10360639 | — |
Reaction Steps
Oxo[3-(2-oxopyrrolidin-1-yl)phenyl]acetaldehyde was reacted with 2,4-difluorobenzenecarboximidic hydrazide hydriodide salt (0.74 g, 2.46 mmol) using the method described in Example 1 to give 1-{3-[3-(2,4-difluorophenyl)-[1,2,4]triazin-5-yl]phenyl}pyrrolidin-2-one as a yellow solid (0.5 g): δH H (400 MHz, d6-DMSO) 2.08-2.16 (2H, m), 2.55 (2H, t, J 8.2 Hz), 3.96 (2H, t, J 7.0 Hz), 7.34-7.39 (1H, m), 7.49-7.56 (1H, m), 7.65 (1H, t, J 8.0 Hz), 8.00-8.03 (1H, m), 8.16 (1H, d, J 7.8 Hz), 8.27-8.33 (1H, m), 8.59 (1H, t, J 1.8 Hz), 10.08 (1H, s); m/z (ES+) 353.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06969716B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-64b81f7ca0444ec38ef98d82e655abed |
| Source note | uspto-grants-2005_11 |