HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Acetylbenzoic Acid → HCID 178418764, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Acetylbenzoic Acid | HCID 11470 | — |
| Reactant | HCID 178418995 | HCID 178418995 | — |
| Product | HCID 178418764 | HCID 178418764 | 60% |
Reaction Steps
The title compound was prepared by condensing 5-(3H-imidazo[4,5-b]pyridin-2-yl)-2,4-dimethoxy-benzaldehyde (Ex-76B) and 4-acetylbenzoic acid in a similar manner as described in Ex-3. Yellow solid, mp 222–224° C., 60% yield. 1H-NMR (DMSO-d6) δ 8.75 (s, 1H), 8.38–8.40 (m, 1H), 8.18 (d, J=9 Hz, 2H), 7.99–8.08 (m, 4H), 7.83 (d, J=15 Hz, 1H), 7.28–7.33 (m, 1H), 6.91 (s, 1H), 4.11 (s, 3H), 4.04 (s, 3H). MS m/z=430 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07094801B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-4d74efb6431442d1af68fd61062acc4e |
| Source note | uspto-grants-2006_08 |