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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596204Generated: October 26, 2026

1-Methyl-5-nitro-1H-imidazole-2-carbaldehyde → N-methyl-1-(1-methyl-5-nitroimidazol-2-yl)methanimine oxide

https://huagongshe.com/reaction/596204

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-5-nitro-1H-imidazole-2-carbaldehydeHCID 78487—
ReactantN-benzylhydroxylamine hydrochlorideHCID 11332622—
Reactantalpha-(1-ethyl-5-nitroimidazol-2-yl)-N-methylnitroneHCID 86734513—
Reactantalpha-(1-propyl-5-nitroimidazol-2yl)-N-methylnitroneHCID 86734514—
Reactantalpha-(1-methyl-5-nitroimidazol-2-yl)-N-benzylnitroneHCID 86734515—
ProductN-methyl-1-(1-methyl-5-nitroimidazol-2-yl)methanimine oxideHCID 302288—

Reaction Steps

The corresponding α-(1-ethyl-5-nitroimidazol-2-yl)-N-methylnitrone, α-(1-propyl-5-nitroimidazol-2yl)-N-methylnitrone, and α[1-(2'-acetoxyethyl)-5-nitroimidazol-2-yl]-N-methylnitrone can be prepared in a similar fashion utilizing the respectively 1-substituted-2-formyl-5-nitroimidazoles disclosed in Examples 3 and 5. 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04010176
Source datasetuspto-grants-1977_03
ORD IDord-5be3636738ed41fca0b18d9339d0073a
Source noteuspto-grants-1977_03