HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine N-Oxide → HCID 13961163, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine N-Oxide | HCID 12753 | — |
| Reactant | 5,6-Dimethyl-1H-benzimidazole-2-methanethiol | HCID 52210 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 13961163 | HCID 13961163 | — |
Reaction Steps
A solution of 3.84 g (0.02 mole) of 5,6-dimethyl-2-mercaptomethylbenzimidazole and 1.9 g (0.02 mole) of pyridine N-oxide in 50 ml of acetic anhydride is heated to 100° C. for 4 hours. The acetic anhydride is evaporated off, the residue taken up with acetone and the mixture filtered and concentrated to a volume of 20 ml. From this solution, 2.6 g (48%) of 5,6-dimethyl-2-(2-pyridylthiomethyl)benzimidazole crystallize. The product thereby obtained is identical to that obtained by Method A, and the data for the identification appear in Tables 1 and 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04791114 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-d15d597944284d1da824907aa9535105 |
| Source note | uspto-grants-1988_12 |