HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphorus oxychloride → HCID 178527396, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | (Phenylsulfonyl)acetic acid | HCID 59543 | — |
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | 1H-benzimidazole-5-carbohydrazide | HCID 16637119 | — |
| Product | HCID 178527396 | HCID 178527396 | — |
Reaction Steps
The compound was synthesized starting from phenylsulfonylacetic acid (201 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: 0.051 G (14.3%); MS m/z: 357.1 [M+H]+; 1H-NMR (DMSO d6, 400 MHz): δ 5.51 (s, 2H); 7.63-7.67 (m, 2H); 7.75-7.77 (m, 1H); 7.84-7.87 (m, 3H); 7.98 (dd, 1H, 4J=1.7 Hz, 3J=8.3 Hz); 8.30 (d, 1H, 4J=1.7 Hz); 8.95 (s, 1H); HPLC (METHOD [A]): rt 10.49 min (98.3%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181233B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-49e861ce348546ff853bf084bd8e5822 |
| Source note | uspto-grants-2015_11 |