HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (E)-5-Fluoro-(4-methoxystyryl)-1-(2-pyridyl)-1H-benzimidazole hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole | HCID 9796241 | — |
| Reactant | trans-4-Methoxycinnamoyl chloride | HCID 10976422 | — |
| Reactant | 4-fluoro-2-amino-N-(2-pyridyl)aniline | HCID 22736745 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (E)-5-Fluoro-(4-methoxystyryl)-1-(2-pyridyl)-1H-benzimidazole hydrochloride | HCID 22736773 | — |
Reaction Steps
Free base of the titled compound was prepared from 4-fluoro-2-amino-N-(2-pyridyl)aniline and (E)-4-methoxycinnamoyl chloride according to the preparation of (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole (Example 1, method A). The free base was treated with a 10% methanol solution of hydrogen chloride and concentrated to dryness. The residue was recrystallized from ethyl acetate/ethanol to give the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06310079B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-0fee7e0766ed4dd59074511224a76655 |
| Source note | uspto-grants-2001_10 |