HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → 3-(4,5-dichloro-1H-imidazol-2-yl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 3-(1H-Imidazol-2-yl)pyridine | HCID 12395500 | — |
| Product | 3-(4,5-dichloro-1H-imidazol-2-yl)pyridine | HCID 21398902 | — |
Reaction Steps
To a suspension of 2-(3-pyridyl)-imidazole (1.5 g., 0.01 moles) in chloroform (150 ml.) is added dropwise with stirring over one hour at reflux N-chlorosuccinimide (2.6 g., 0.02 moles). The reaction mixture is heated three hours at reflux. After cooling, the solvent is removed at 20 mm. and the residue triturated with water while heating on a steam bath. The resulting solid is filtered and after recrystallization from acetonitrile 400 mg. of 2-(3-pyridyl)-4,5-dichloroimidazole is obtained, m.p. 237°-238° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04058614 |
| Source dataset | uspto-grants-1977_11 |
| ORD ID | ord-6b62ec7126eb43fb85506213ab94d354 |
| Source note | uspto-grants-1977_11 |