HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazald → HCID 53379980, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazald | HCID 6628 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 21225595 | HCID 21225595 | — |
| Reactant | HCID 67387260 | HCID 67387260 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 53379980 | HCID 53379980 | — |
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)-5-cyclohexyl-3-hydroxy-4-methyl-1H-pyrrol-2(5H)-one (1.00 g, 3.22 mmol, 1 eq) and MeOH (10 ml); yield: 0.250 g (25%); MS m/z: 326.1 [M+H]+; 1H-NMR: (400 MHz, DMSO-D6) δ: 1.05 (d, 3H), 1.40 (d, 2H), 1.65-1.60 (m, 4H), 2.05 (s, 3H), 4.03 (s, 3H), 4.40 (s, 1H), 7.05 (s, 1H), 7.62 (s, 1H), 7.63 (s, 1H), 7.82 (s, 1H); HPLC (METHOD [A]): rt 11.25 min (98.78%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08269019B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-69d12e5dba8741a59a0c3931b213632c |
| Source note | uspto-grants-2012_09 |