HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methyl-5-nitro-1H-imidazole-2-carbaldehyde → N-methyl-1-(1-methyl-5-nitroimidazol-2-yl)methanimine oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methyl-5-nitro-1H-imidazole-2-carbaldehyde | HCID 78487 | — |
| Reactant | N-benzylhydroxylamine hydrochloride | HCID 11332622 | — |
| Reactant | alpha-(1-methyl-5-nitroimidazol-2-yl)-N-benzylnitrone | HCID 86734515 | — |
| Product | N-methyl-1-(1-methyl-5-nitroimidazol-2-yl)methanimine oxide | HCID 302288 | — |
Reaction Steps
The corresponding α-(1-methyl-5-nitroimidazol-2-yl)-N-benzylnitrone can also be prepared using N-benzylhydroxylamine hydrochloride in the above reaction with 1-methyl-2-formyl-5-nitroimidazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04080340 |
| Source dataset | uspto-grants-1978_03 |
| ORD ID | ord-f4c1d66eaf1e42f4907d760df652e0e2 |
| Source note | uspto-grants-1978_03 |