HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Nitroacetophenone → HCID 88069650, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Nitroacetophenone | HCID 7487 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Glycine, N-(2-chloronicotinoyl)- | HCID 53558 | — |
| Reactant | HCID 178418268 | HCID 178418268 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 88069650 | HCID 88069650 | 20.8% |
Reaction Steps
A mixture of 2-{[(2-chloro-3-pyridinyl)carbonyl]amino}acetic acid (6.44 g, 30 mmol, prepared from glycine and 2-chloronicotinoyl chloride), 4-nitroacetophenone (2.48 g, 15 mmol), lead (IV) acetate (3.33 g, 7.5 mmol) and acetic anhydride in THF (30 ml) was heated at reflux for 4 days. The mixture was poured onto crushed ice, the solid filtered off, washed with water and dried. The brown solid was triturated twice with boiling ethanol and filtered off to give the title compound as a brown solid (1.07 g). δH (CDCl3), 8.57 (1H, dd, J 4.8, 2.1 Hz, PyH), 8.34-8,29 (3H, m, ArH+PyH), 8.05 (2H, d, J 9.1 Hz, ArH), 7.41 (1H, dd, J 7.9, 4.8 Hz, PyH) and 2.84 (3H, s, Me).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06465471B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-4f34db70fe8f424a802c52c2d1c949a8 |
| Source note | uspto-grants-2002_10 |