HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazald → HCID 53380166, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazald | HCID 6628 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 21225595 | HCID 21225595 | — |
| Reactant | HCID 67387552 | HCID 67387552 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 53380166 | HCID 53380166 | — |
Reaction Steps
The compound was synthesized starting from KOH (15 eq in water), diazald (8 eq), ethylene glycol/Et2O (1/4.2 v/v, 31 ml), 1-(1H-Benzo[d]imidazol-6-yl)-5-(2,3-difluorophenyl)-4-(4-fluorophenyl)-3-hydroxy-1H-pyrrol-2(5H)-one (0.5 g, 1.2 mmol, 1 eq) and MeOH (10 ml); yield: 0.160 g (60%); MS m/z: 436.1 [M+H]+; 1H-NMR: (400 MHz, DMSO-D6) δ: 10.5 (b, 1H), 7.88 (s, 1H), 7.72 (s, 1H), 7.59-7.56 (m, 1H), 7.26-7.00 (m, 4H), 6.91-6.86 (m, 3H), 6.38 (bs, 1H), 4.20 (s, 3H); HPLC (METHOD [A]): rt 15.20 min (97.35%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08420828B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-6958c2a4447c47eb911fa27e2be9d883 |
| Source note | uspto-grants-2013_04 |