HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 3-(4-Methyl-5-(methylthio)-4H-1,2,4-triazol-3-yl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-methyl-5-(pyridin-3-yl)-4H-1,2,4-triazole-3-thiol | HCID 757582 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(4-Methyl-5-(methylthio)-4H-1,2,4-triazol-3-yl)pyridine | HCID 40424626 | 98% |
Reaction Steps
MeI (2 mL, 32 mmol) in EtOH (10 mL) was added to a mixture of 4-methyl-5-pyridin-3-yl-2,4-dihydro-3H-1,2,4-triazole-3-thione in 1 M NaOH (70 mL, 70 mmol). After 1 h stirring at r.t., DCM was added and the layers were separated. The water phase was washed with DCM and the combined organic phases were dried and concentrated to give 6.5 g (98%) of the title compound. 1H NMR: 2.76 (s, 3H) 3.59 (s, 3H) 7.43 (m, 1H) 7.99 (m, 1H) 8.71 (m, 1H) 8.86 (m, 1H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07691892B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-454afc4cafe04330ba1f1e96423e8467 |
| Source note | uspto-grants-2010_04 |