Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 1,1'-Thiocarbonyldiimidazole | HCID 80264 | — |
| Reactant | 3-Hydrazinyl-6-(1-methyl-1H-pyrazol-4-yl)pyridazine | HCID 58075172 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178480034 | HCID 178480034 | 60% |
Reaction Steps
[6-(1-Methyl-1H-pyrazol-4-yl)-pyridazin-3-yl]-hydrazine (1.0 g, 5.3 mmol) and 1,1′-thiocarbonyldiimidazole (1.08 g, 6.1 mmol) were combined in DMF (10 mL) and heated at 50° C. for 2 h. After such time the mixture was allowed to cool to room temperature. Hexane (10 mL) was added followed by THF (4 mL), stirred for 10 mins then filtered and washed with THF (2 mL then 4 mL). Solid dried in vacuo to return 738 mg of 6-(1-methyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[4,3-b]pyridazine-3-thiol as a yellow solid (60% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507489B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-c7fd008ca4ed46aea2db9aef0ae8c665 |
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| Source note | uspto-grants-2013_08 |
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