HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazine → 3-Chloro-6-ethoxy[1,2,4]triazolo[4,3-b]pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazine | HCID 1482346 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Chloro-6-ethoxy[1,2,4]triazolo[4,3-b]pyridazine | HCID 67524522 | — |
Reaction Steps
The 3-chloro-6-ethoxy[1,2,4]triazolo[4,3-b]pyridazine was prepared according to the method described in Example 16b, but using 1 g of commercial 3,6-dichloro[1,2,4]triazolo[4,3-b]pyridazine, 1.71 g of a solution at 21% of sodium ethoxide in ethanol and 30 cm3 of dioxane, after reaction at reflux for 5.5 h. 874 mg of 3-chloro-6-ethoxy[1,2,4]triazolo[4,3-b]pyridazine are thus obtained in the form of a whitish powder, the characteristics are as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321777B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-f6a03f1af259489c9469e54f6e0242d8 |
| Source note | uspto-grants-2016_04 |