HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphorus oxychloride → HCID 178505669, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | 3,4-Difluorohydrocinnamic acid | HCID 2778994 | — |
| Reactant | 1H-benzimidazole-5-carbohydrazide | HCID 16637119 | — |
| Product | HCID 178505669 | HCID 178505669 | — |
Reaction Steps
The compound was synthesized starting from 3-(3,4-difluorophenyl)propionic acid (186 mg; 1 mmol), benzimidazol-5-carbohydrazide (176 mg; 1 mmol), Lawesson's reagent (606 mg; 1.5 mmol) and POCl3 (0.137 ml; 1.5 mmol) as described in method 3; yield: 0.02 g (5.8%); MS m/z: 343.3 [M+H]+; 1H-NMR (DMSO d6, 400 MHz): δ 3.11 (t, 2H, 3J=7.5 Hz); 3.47 (t, 2H, 3J=7.5 Hz); 6.97-6.99 (m, 1H); 7.32-7.35 (m, 1H); 7.40-7.46 (m, 1H); 7.82 (d, 1H, 3J=8.7 Hz); 7.91 (dd, 1H, 4J=1.7 Hz, 3J=8.7 Hz); 8.22 (d, 1H, 4J=1.7 Hz), 8.87 (s, 1H); HPLC (METHOD [A]): rt 13.09 min (85.7%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181233B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-12ae1729aed242c384bcf4be1bb03653 |
| Source note | uspto-grants-2015_11 |