HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Acetylbenzoic Acid → 4-{3E-[2,4-Dimethoxy-5-(1-methyl-1H-indol-2-yl)-phenyl]-acryloyl}-benzoic acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Acetylbenzoic Acid | HCID 11470 | — |
| Edukt | 2,4-dimethoxy-5-(1-methyl-1H-indol-2-yl)benzaldehyde | HCID 21981006 | — |
| Produkt | 4-{3E-[2,4-Dimethoxy-5-(1-methyl-1H-indol-2-yl)-phenyl]-acryloyl}-benzoic acid | HCID 10173610 | 87% |
Reaktionsschritte
The title compound was prepared by condensing 4-acetylbenzoic acid and 2,4-dimethoxy-5-(1-methyl-1H-indol-2-yl)-benzaldehyde (Ex-116A) in a similar manner as described in Ex-3. Yellow solid, 87% yield, mp 157–160° C. 1H-NMR (DMSO-d6) δ 8.17 (d, J=8 Hz, 2H), 8.08 (d, J=15 Hz, 1H), 7.99–9.02 (m 3H), 7.83 (d, J=15 Hz, 1H), 7.52 (d, J=8 Hz, 1H), 7.42 (d, J=8 Hz, 1H), 7.10–7.15 (m, 1H), 6.99–7.04 (m, 1H), 6.85 (s, 1H), 6.42 (s, 1H), 4.01 (s, 3H), 3.88 (s, 3H), 3.50 (s, 3H). MS m/z=442 ([M+H]+, 100%). HRMS (ES+) Calcd. for C27H23NO5: 442.1654. Found: 442.1633.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07094801B2 |
| Quelldatensatz | uspto-grants-2006_08 |
| ORD ID | ord-df24f20e04da4cf9bb28b80952681e46 |
| Quellennotiz | uspto-grants-2006_08 |