Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Anthranilic Acid | HCID 227 | — |
| Edukt | Triphenyl phosphite | HCID 7540 | — |
| Edukt | P-Anisidine | HCID 7732 | — |
| Edukt | 3-Phthalimidopropionic acid | HCID 76859 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | HCID 1366773 | HCID 1366773 | — |
Reaktionsschritte
Anthranilic acid (2.0 g, 14.6 mmol), 3-phthalimidopropionic acid (3.2 g, 14.6 mmol), and triphenylphosphite (4.0 mL, 15.3 mmol) were dissolved in pyridine (20 mL) and heated in a sealed tube at 100° C. for 2 hours. After cooling to room temperature, the tube was opened, p-anisidine (2.7 g, 21.9 mmol) was added and heating at 100° C. was resumed for 4 hours. The pyridine was removed by azeotroping with toluene, and the residue was suspended in CHCl3 and toluene. The solids that crashed out were removed, and the residue was purified by silica gel chromatography with gradient elution (0 to 100% EtOAc in hexanes). A white solid precipitated from several of the fractions which was isolated by filtration to provide A-1 (2.23 g, 36%). Data for A-1: LRMS: calculated M+H for C25H19N3O4: 426.14. Found: 426.16.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08846000B2 |
|---|
| Quelldatensatz | uspto-grants-2014_09 |
|---|
| ORD ID | ord-62ca15e8a0a44407b015f3ebc78576e5 |
|---|
| Quellennotiz | uspto-grants-2014_09 |
|---|