HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Anthranilic Acid → HCID 69510389, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Anthranilic Acid | HCID 227 | — |
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 7-Fluoro-1H-indole-3-carbaldehyde | HCID 22139120 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | HCID 69510389 | HCID 69510389 | — |
Reaktionsschritte
A mixture of 7-fluoro-1H-indole-3-carbaldehyde (200 mg, 1.23 mmol), 2-amino-benzoic acid (168 mg, 1.23 mmol) and p-toluenesulfonic acid (20 mg, 10% W/W) was heated a reflux in toluene (5 mL) for 4 h. The mixture was cooled to RT and diluted with CH2Cl2. NaBH4 (51.4 mg) was added followed by MeOH (2 mL). The mixture was stirred for 1 h. The reaction mixture was diluted with EtOAc (10 mL) and extracted with water (2×10 mL). The organic layer was dried over Na2SO4 and concentrated in vacuo affording the titled compound as a light yellow solid. ESI MS: (M−1)=283. Calc'd for C16H13FN2O2-284.29.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07307088B2 |
| Quelldatensatz | uspto-grants-2007_12 |
| ORD ID | ord-bdf5aee18ed2430f9455e6152b5c501a |
| Quellennotiz | uspto-grants-2007_12 |