HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexylamine → 2-(2-Cyclohexylamino-5-thiadiazolyl)-1-methyl-5nitroimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | 2-(2-Chloro-5-thiadiazolyl)-1-methyl-5-nitroimidazole | HCID 21390801 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(2-Cyclohexylamino-5-thiadiazolyl)-1-methyl-5nitroimidazole | HCID 21390861 | — |
Reaction Steps
A mixture of 5.0 g. of 2-(2-chloro-5-thiadiazolyl)-1-methyl-5-nitroimidazole, 6.0 g. of cyclohexylamine and 125 ml. of dioxane is stirred at reflux until thin-layer chromatographic analysis indicates that the chloro intermediate is completely utilized. The dioxane is removed under reduced pressure and the residue triturated with aqueous sodium bicarbonate solution. Recrystallization from a mixture of ethylacetate and acetone yields the pure compound melting at 215°-217° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04065567 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-adcb9dcdcc804a23b2b12019b726ef8a |
| Source note | uspto-grants-1977_12 |