HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lawesson's reagent → HCID 178490027, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | 2,4-Dimethoxyphenylpropionylchloride | HCID 15179939 | — |
| Reactant | 1H-benzimidazole-5-carbohydrazide | HCID 16637119 | — |
| Product | HCID 178490027 | HCID 178490027 | — |
Reaction Steps
The compound was synthesized starting from benzimidazol-5-carbohydrazide (176 mg; 1 mmol), TEA (0.153 ml; 1.1 mmol), 2,4-dimethoxyphenylpropionylchloride (228 mg, 1.1 mmol) and Lawesson's reagent (606 mg; 1.5 mmol) as described in method 1; yield: 0.022 g (6.0%); MS m/z: 367.2 [M+H]+; 1H-NMR (DMSO d6, 400 MHz): δ 2.94 (t, 2H, 3J=7.9 Hz); 3.30 (t, 2H, 3J=7.9 Hz); 3.70 (s, 3H); 3.74 (s, 3H); 6.41 (dd, 1H, 4J=2.5 Hz, 3J=8.3 Hz); 6.51 (d, 1H, 4J=2.5 Hz); 7.05 (d, 1H, 3J=8.3 Hz); 7.68 (d, 1H, 3J=8.7 Hz); 7.74 (dd, 1H, 4J=1.7 Hz, 3J=8.7 Hz); 8.09 (br s, 1H); 8.34 (s, 1H); HPLC (METHOD [A]): rt 12.63 min (97.6%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181233B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-2e1129437dd248a480bfc64df70e1102 |
| Source note | uspto-grants-2015_11 |