HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 6-chloro-2-methyl[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-chloro-2H,3H-[1,2,4]triazolo[4,3-b]pyridazin-3-one | HCID 6407182 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-chloro-2-methyl[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-one | HCID 23000328 | 67.2% |
Reaction Steps
0.853 g of 6-chloro[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-one was dissolved in 5 ml of N,N-dimethylformamide; 0.83 g of potassium carbonate was added; with stirring at room temperature, 0.5 ml of methyl iodide was added. After stirring at room temperature for 15 hours, ice water and saline were added; the reaction mixture was extracted with ethyl acetate-tetrahydrofuran (1:1); the extract was washed with saline and dried over magnesium sulfate. After concentration under reduced pressure, the crystal obtained was collected by filtration, washed with diethyl ether, and dried, to yield 0.62 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06610694B1 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-809f861659cd41a7b0f787210052c141 |
| Source note | uspto-grants-2003_08 |