HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazald → HCID 53380361, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazald | HCID 6628 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 21225595 | HCID 21225595 | — |
| Reactant | HCID 67387227 | HCID 67387227 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 53380361 | HCID 53380361 | — |
Reaction Steps
The compound was synthesized starting from KOH (15 eq in water), diazald (8 eq), ethylene glycol/Et2O (1/2 v/v, 30 ml), 1-(1H-Benzo[d]imidazol-6-yl)-3-hydroxy-4-methyl-5-(4-(4-morpholinocyclohexyl)phenyl)-1H-pyrrol-2(5H)-one (0.350 g, 0.74 mmol, 1 eq) and MeOH (10 ml); yield: 0.040 g (11%); MS m/z: 487.2 [M+H]+; 1H-NMR: (400 MHz, CDCl3) δ: 12.34 (s, 1H), 8.13 (d, 1H), 7.70 (d, 1H), 7.45 (d, 2H), 7.17 (d, 5H), 5.75 (s, 1H), 3.95 (s, 3H), 3.56 (d, 4H), 2.35 (d, 4H), 2.1 (d, 1H), 1.90 (d, 2H), 1.69 (d, 5H), 1.4 (d, 4H); HPLC (METHOD [A]): rt 7.84 min (98.72%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08269019B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-b220d48b1ff14410ad23c107bfa2f8b2 |
| Source note | uspto-grants-2012_09 |