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 | 3,6-Dichloropyridazine | HCID 67331 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | 3-Chloro-6-(1H-imidazol-1-yl)pyridazine | HCID 2770903 | 38% |
Reaction Steps
A solution of 3,6-dichloropyridazine (Aldrich, 300 mg, 2.0 mmol), imidazole (Aldrich, 163 mg, 2.4 mmol), and diisopropylethylamine (620 mg, 4.8 mmol) in 1.5 mL 1,2-dichlorobenzene was heated in a sealed tube to 120° C. at 330 watts for 45 min in an Emry™ Creator microwave. The crude reaction mixture was purified by column chromatography (SiO2, 1% methanol-CH2Cl2) to give 135 mg of the title compound (0.75 mmol, 38% yield) as the major product. MS (DCl/NH3) m/z 181 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07872010B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-2529d6304e2f446c96f5317e1d234d4f |
| Source note | uspto-grants-2011_01 |