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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloro-2-methyl-3-nitrosobutane | HCID 10866386 | — |
| Reactant | 1-[3-amino-2-(aminooxy)propyl]-2-nitro-1H-imidazole dihydrochloride | HCID 11288810 | — |
| Product | 3,3,9,9-tetramethyl-6-[(2-nitro-1H-imidazol-1-yl)methyl]-5-oxa-4,8-diazaundecane-2,10-dione dioxime | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06933391B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-d986145f82454b8aa87f93d92dd446d2 |
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| Source note | uspto-grants-2005_08 |
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