HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dazoxiben → HCID 9913269, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dazoxiben | HCID 53001 | — |
| Reactant | HCID 16793499 | HCID 16793499 | — |
| Product | HCID 9913269 | HCID 9913269 | 75% |
Reaction Steps
Using an analogous procedure to that described in Example 14, N-(3-amino-4-chlorophenyl)-4-cyanobenzamide was reacted with 4-[2-(imidazol-1-yl)ethoxy]benzoic acid (J. Med. Chem., 1985, 28, 1427) to give the title compound in 75% yield; NMR Spectrum: (DMSOd6) 4.48 (t, 2H), 4.65 (m, 2H), 7.09 (d, 1H), 7.51 (d, 1H), 7.68 (m, 3H), 7.82 (s, 1H), 8.0 (m, 4H), 8.1 (m, 2H), 8.73 (d, 1H), 9.18 (s, 1H), 9.89 (s, 1H), 10.66 (s, 1H); Mass Spectrum: M−H− 484.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06579872B1 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-902a723b415f432aae3b12676c21846e |
| Source note | uspto-grants-2003_06 |