HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazald → HCID 53380266, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazald | HCID 6628 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 21225595 | HCID 21225595 | — |
| Reactant | HCID 67387564 | HCID 67387564 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 53380266 | HCID 53380266 | — |
Reaction Steps
The compound was synthesized starting from KOH (15 eq in water), diazald (9 eq), ethylene glycol/Et2O (1/2 v/v, 30 ml), 1-(1H-Benzo[d]imidazol-6-yl)-5-(4-cyclohexylphenyl)-3-hydroxy-4-methyl-1H-pyrrol-2(5H)-one (0.900 g, 2.32 mmol, 1 eq) and MeOH (10 ml); yield: 0.200 g (21.4%); MS m/z: 402.1 [M+H]+; 1H-NMR: (400 MHz, DMSO-D6) δ: 12.4 (b, 1H), 8.32 (s, 1H), 7.71 (s, 1H), 7.46-7.44 (m, 1H), 7.34 (m, 1H), 7.16-7.11 (m, 4H), 5.77 (s, 1H), 3.93 (s, 3H), 2.39 (m, 1H), 1.79-1.60 (m, 8H), 1.40-1.20 (m, 6H); HPLC (METHOD [A]): rt 15.68 min (96.92%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08269019B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-3a18726f1100445e9d925c94cadd725b |
| Source note | uspto-grants-2012_09 |