HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Acetylbenzenesulphonamide → HCID 178419065, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Acetylbenzenesulphonamide | HCID 74065 | — |
| Reactant | HCID 178418995 | HCID 178418995 | — |
| Product | HCID 178419065 | HCID 178419065 | 26% |
Reaction Steps
The title compound was prepared by condensing 5-(3H-imidazo[4,5-b]pyridin-2-yl)-2,4-dimethoxy-benzaldehyde (Ex-76A) with 4-acetyl-benzenesulfonamide (Ex-26A) in a similar manner as described in Ex-22. Yellow solid, 26% yield, mp>260° C. 1H-NMR (DMSO-d6) δ 8.73 (s, 1H), 8.31 (dd, J=1, 4 Hz, 1H), 8.26 (d, J=8 Hz, 2H), 8.05 (d, J=16 Hz, 1H), 7.89–7.97 (m, 3H), 7.82 (d, J=16 Hz, 1H), 7.17–7.21 (m, 1H), 6.89 (s, 1H), 4.09 (s, 3H), 4.03 (s, 3H). MS m/z=465([M+H]+, 65%), 256 (100%). HRMS (ES+) Calcd. for C23H20N4O5S: 465.1232. Found: 465.1240.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07094801B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-2d24683324d84ddc92f92a2159bf2ee5 |
| Source note | uspto-grants-2006_08 |