Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Pyridinemethanamine | HCID 77317 | — |
| Reactant | HCID 14990940 | HCID 14990940 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 14518708 | HCID 14518708 | 61% |
Reaction Steps
A mixture of 13.2 parts of 1-[(4-fluoro-3-nitrophenyl)methyl]-1H-imidazole, 13 parts of 4-pyridinemethanamine and 80 parts of ethanol was stirred for 6 hours at 60° C. 14.5 Parts of sodium hydroxide were added and the whole was stirred for 30 minutes at 60° C. The reaction mixture was evaporated. The residue was dissolved in 100 parts of water. Hydrochloric acid was added dropwise till a pH between 6 and 7 was reached. The product was filtered off, washed with water and 2-propanol and crystallized from 80 parts of 2-propanol. The product was filtered off and dried, yielding 10.7 parts (61%) of 6-(1H-imidazol-1-ylmethyl)-2-(4-pyridinyl)-1H-benzimidazol-1-ol; mp. 198.1° C. (compound 209).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04859684 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-254ba9a49f55421ea55122dd94f44b90 |
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| Source note | uspto-grants-1989_08 |
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