HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrobenzene → HCID 178458251, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | Acetonitrile ether | HCID 21885917 | — |
| Reactant | 3,4-Diaminobenzimidamide hydrochloride | HCID 22125532 | — |
| Product | HCID 178458251 | HCID 178458251 | — |
Reaction Steps
A mixture comprising 5-propoxypyridine-2-carboxyaldehyde (0.19 g, 1.15 mmol), 3,4-diaminobenzamidine hydrochloride (0.21 g, 1.15 mmol) and nitrobenzene (2 mL) was heated at 150° C. for 15 hours, cooled and then diluted with 1:1 acetonitrile/ether (50 mL) to give a precipitate. The precipitate was isolated by filtration and purified by HPLC to provide 2-(5-propyloxypyridin-2-yl]-1H-benzimidazole-5-carboxamidine. 1H-NMR (300 Mhz, CD3OD): 1.1 (t, 3H), 2.0 (m, 2H), 4.5 (t, 2H), 7.75 (m, 1H), 7.86 (m, 2H), 8.1 (m, 1H), 8.35 (m, 1H); 8.55 (m, 1H); MS (ESI), Calculated for C16H17N5O: 295.3, Found (MH+): 295.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06150379 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-fc682aa69d8f4f1c8e6e41ff40afcd5a |
| Source note | uspto-grants-2000_11 |