HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazald → HCID 53380263, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazald | HCID 6628 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 21225595 | HCID 21225595 | — |
| Reactant | HCID 67386994 | HCID 67386994 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 53380263 | HCID 53380263 | — |
Reaction Steps
The compound was synthesized starting from KOH (15 eq in water), diazald (8 eq), ethylene glycol/Et2O (1/2 v/v, 60 ml), 1-(1H-Benzo[d]imidazol-6-yl)-3-hydroxy-4-methyl-5-(4-(piperidin-1-yl)phenyl)-1H-pyrrol-2(5H)-one (0.700 g, 1.88 mmol, 1 eq) and MeOH (20 ml); yield: 0.050 g (7%); MS m/z: 403.1 [M+H]+; 1H-NMR: (400 MHz, DMSO-D6) δ: 8.59 (s, 1H), 7.81 (s, 1H), 7.55-7.53 (m, 1H), 7.45-7.42 (m, 1H), 7.06-7.04 (m, 2H), 6.82-6.79 (m, 2H), 5.69 (s, 1H), 3.93 (s, 3H), 3.05-3.02 (m, 4H), 1.70 (s, 3H), 1.53-1.46 (m, 6H); HPLC (METHOD [A]): rt 6.03 min (99.04%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08420828B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-6518125ea6f44279810eafde428efcd5 |
| Source note | uspto-grants-2013_04 |