HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 3-Chloro-6-(1H-imidazol-1-yl)pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,6-Dichloropyridazine | HCID 67331 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Chloro-6-(1H-imidazol-1-yl)pyridazine | HCID 2770903 | 83.1% |
Reaction Steps
A mixture of imidazole (0.613 g, 8 mmol) and 3,6-dichloropyridazine (1.55 g, 10 mmol), K2CO3 (4.15 g) and DMF (15 mL) was heated at 70–80° C. overnight. After removal of DMF in vacuo, the residual solid was dissolved in CH2Cl2 (50 mL), washed with 1N Na2CO3 aq. solution, and dried (MgSO4). Separation using column chromatography (CH2Cl2/methanol 100:1) afforded 3-chloro-6-(imidazol-1-yl)pyridazine (1.2 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07202263B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-73bfa0823ce540c7a2ff9893e3bd240f |
| Source note | uspto-grants-2007_04 |