HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21432236, compound → HCID 21432233, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21432236 | HCID 21432236 | — |
| Reactant | HCID 21432257 | HCID 21432257 | — |
| Reactant | HCID 21432273 | HCID 21432273 | — |
| Product | HCID 21432233 | HCID 21432233 | — |
| Product | HCID 178462844 | HCID 178462844 | — |
Reaction Steps
In a similar manner, 4,4-dimethyl-1-(1-methyl-5-nitro-2-imidazolecarboximidoyl)-3-thiosemicarbazide, 4-methyl-1-(1-methyl-5-nitro-2-imidazolecarboximidoyl)-3-thiosemicarbazide and 1-(1-[2-hydroxyethyl]-5-nitro-2-imidazolecarboximidoyl)-3-thiosemicarbazide yield respectively, 2-(2-dimethylamino-1,3,4-thiadiazol-5-yl)-1-methyl-5-nitroimidazole (VIIIE), 2-(2-methylamino-1,3,4-thiadiazol-5-yl)-1-methyl-5-nitroimidazole (VIIIC) and 2-(2-amino-1,3,4-thiadiazol-5-yl)-1-(2-hydroxyethyl)-5-nitroimidazole (VIIID). According to the above procedure, 2-(2-amino-1,3,4-thiadiazol-5-yl)-1-ethyl-5-nitroimidazole (VIIIE) is obtained from 1-(1-ethyl-5-nitro-2-imidazolecarboximidoyl)-3-thiosemicarbazide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04026903 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-4139b34541284db197621dc4f985cce1 |
| Source note | uspto-grants-1977_05 |