HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Thiosulfate → 2-{[[4-(2-Furylmethylthio)-3-methyl-2-pyridinyl]methyl]sulfinyl}-1H-benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | 2-{[[4-(2-Furylmethylthio)-3-methyl-2-pyridinyl]methyl]thio}-1H-benzimidazole | HCID 9799366 | — |
| Reactant | NaOH dioxane | HCID 18323598 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Product | 2-{[[4-(2-Furylmethylthio)-3-methyl-2-pyridinyl]methyl]sulfinyl}-1H-benzimidazole | HCID 23363027 | 80% |
Reaction Steps
2-{[[4-(2-Furylmethylthio)-3-methyl-2-pyridinyl]methyl]thio}-1H-benzimidazole (2 mmol) are dissolved in 15 ml of dioxane + NaOH (6 mmol; 2N), and the solution is treated with 2.5 mmol of 7 percent strength sodium hypochlorite solution at 20° C. Sodium thiosulfate is added, dioxane is distilled off, the pH is brought to 9, the mixture is extracted using dichloromethane, and the product is crystallized from dichloromethane/diisopropyl ether. This gives the title compound (yield 80%) of m.p. 173° C. (decomp.) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05587389 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-09a92c57475041feb85166973aedb692 |
| Source note | uspto-grants-1996_12 |