HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazald → HCID 53380363, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazald | HCID 6628 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 21225595 | HCID 21225595 | — |
| Reactant | HCID 67387537 | HCID 67387537 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 53380363 | HCID 53380363 | — |
Reaction Steps
The compound was synthesized starting from KOH (15 eq in water), diazald (9 eq), ethylene glycol/Et2O (1/5 v/v, 18 ml), 1-(1H-Benzo[d]imidazol-6-yl)-3-hydroxy-4-methyl-5-(1-phenylpiperidin-4-yl)-1H-pyrrol-2(5H)-one (0.280 g, 0.72 mmol, 1 eq) and MeOH (15 ml), the product was further purified by prep TLC; yield: 0.021 g (5.2%); MS m/z: 403.1 [M+H]+; 1H-NMR: (400 MHz, CDCl3) δ: 7.95 (s, 1H), 7.65-7.60 (m, 1H), 7.17 (m, 3H), 6.80 (d, 1H), 4.52 (s, 1H), 4.03 (s, 3H), 3.69-3.66 (m, 3H), 2.54-2.41 (m, 3H), 2.05 (s, 4H), 1.88 (m, 5H), 1.41-1.25 (m, 2H); HPLC (METHOD [A]): rt 6.05 min (88.89%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08420828B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-87401ca30b4249dc8f574303045b8a9b |
| Source note | uspto-grants-2013_04 |