Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Anthranilic Acid | HCID 227 | — |
| Edukt | 3-Amino-4-hydroxypyridine | HCID 233392 | — |
| Produkt | HCID 23540710 | HCID 23540710 | 39,3% |
Reaktionsschritte
3-Amino-4-hydroxypyridine (2.225 g, 20.0 mmol) and 2-aminobenzoic acid (2.740 g, 20.0 mmol) were stirred in polyphosphoric acid (40 mL) at 140° C. for 6 hrs. The reaction mixture was poured into distilled water and sodium hydroxide was added until pH=8. The precipitate was collected by filtration and the crude product was purified by chromatography on silica gel eluting with petroleum ether:ethyl acetate:Et3N (160:40:1) to give 2-(oxazolo[4,5-c]pyridin-2-yl)benzenamine (1.659 g, Yield: 39%). 1H NMR (400 MHz, DMSO-d6) δ: 6.68 (1H, t, J=7.6 Hz), 6.93 (1H, d, J=8.0 Hz), 7.17 (2H, s), 7.30 (1H, t, J=7.6 Hz), 7.83 (1H, d, J=5.6 Hz), 7.90 (1H, d, J=8.0 Hz), 8.55 (1H, d, J=5.6 Hz), 9.05 (1H, s); MS (ESI) calcd. for C12H9N3O (m/z): 211. found: 212 [M+1]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08088928B2 |
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| Quelldatensatz | uspto-grants-2012_01 |
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| ORD ID | ord-89d9006bfad24159940d030983ed4e04 |
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| Quellennotiz | uspto-grants-2012_01 |
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