HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazald → HCID 178486597, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazald | HCID 6628 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 21225595 | HCID 21225595 | — |
| Reactant | HCID 57923923 | HCID 57923923 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | HCID 178486597 | HCID 178486597 | — |
Reaction Steps
The compound was synthesized starting from KOH (10 eq in water), diazald (5 eq), ethylene glycol/Et2O (3/1 v/v), 1-(1H-benzo[d]imidazol-6-yl)-5-(2,3,5-trifluorophenyl)-3-hydroxy-4-phenyl-1H-pyrrol-2(5H)-one (0.230 g, 0.5 mmol, 1 eq) and MeOH/H2O (90/10 v/v); yield: 0.015 g (6.9%); MS m/z: 436.4 [M+H]+; 1H-NMR: (400 MHz, DMSO-D6) δ: 4.11 (s, 1H), 6.94 (s, 1H), 7.22-7.42 (m, 6H), 7.58-7.68 (m, 3H), 7.73-7.76 (m, 1H), 7.95 (s, 1H), 9.07 (s, 1H); HPLC (METHOD [A]): rt 15.38 min (82%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08420828B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-860d1797b06543ef848b627b6c7bb32f |
| Source note | uspto-grants-2013_04 |