Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585778Generated: October 26, 2026

2-Chloro-2-methyl-3-nitrosobutane → 3,3,9,9-tetramethyl-6-[(2-nitro-1H-imidazol-1-yl)methyl]-5-oxa-4,8-diazaundecane-2,10-dione dioxime

https://huagongshe.com/reaction/585778

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-2-methyl-3-nitrosobutaneHCID 10866386—
Reactant1-[3-amino-2-(aminooxy)propyl]-2-nitro-1H-imidazole dihydrochlorideHCID 11288810—
Product3,3,9,9-tetramethyl-6-[(2-nitro-1H-imidazol-1-yl)methyl]-5-oxa-4,8-diazaundecane-2,10-dione dioximeHCID 72595966—

Reaction Steps

According to the General Reaction Scheme, N-(2,3-epoxypropyl)phthalimide (1) is reacted with 2-nitro-imidazole (2) to obtain 2-[2-Hydroxy-2-(2-nitro-1H-imidazol-1-yl)ethyl]-1H-isoindole-1,3(2H)-dione (3). This product is then reacted with N-hydroxyphthalimide, preferably in the presence of a tertiary amine such as triphenylphosphine, to obtain the intermediate of Formula II, 2-{2-(1,3-dioxoisoindolin-2-yl)-1-[(2-nitroimidazolyl)methyl]ethoxy}isoindoline-1,3-dione (4). This intermediate is then reacted with hydrazine to obtain 1-[3-amino-2-(aminooxy)propyl]-2-nitro-1H-imidazole dihydrochloride (5), which is then reacted with the compound of Formula III to yield the compound of Formula I. A preferred compound of Formula III is 3-chloro-3-methyl-2-nitrosobutane, which, when used contacted with 1-[3-amino-2-(aminooxy)propyl]-2-nitro-1H-imidazole dihydrochloride (5), yields 3,3,9,9-tetramethyl-6-[(2-nitro-1H-imidazol-1-yl)methyl]-5-oxa-4,8-diazaundecane-2,10-dione dioxime (7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06933391B2
Source datasetuspto-grants-2005_08
ORD IDord-d986145f82454b8aa87f93d92dd446d2
Source noteuspto-grants-2005_08