HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968161Generated: October 28, 2026
Diisopropylethylamine → 3,3,9,9-Tetramethyl-1-(4-methyl-2-nitro-1H-imidazol-1-yl)-4,8-diazaundecane-2,10-dione dioxime
https://huagongshe.com/reaction/968161
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Chloro-3-methyl-2-nitroso-1-(4-methyl-2-nitro-1H-imidazol-1-yl)butane | HCID 15185995 | — |
| Reactant | N-(3-aminopropyl)-1-amino-1,1-dimethyl-2-butanone oxime | HCID 86585151 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3,3,9,9-Tetramethyl-1-(4-methyl-2-nitro-1H-imidazol-1-yl)-4,8-diazaundecane-2,10-dione dioxime | HCID 85065087 | — |
Reaction Steps
3-Chloro-3-methyl-2-nitroso-1-(4-methyl-2-nitro-1H-imidazol-1-yl)butane (3.41 g, 13.09 mmol) was added in portions to a stirred solution of N-(3-aminopropyl)-1-amino-1,1-dimethyl-2-butanone oxime (2.0 g, 11.56 mmol, Example 1) and (i-Pr)2NEt (1.64 g, 13.09 mmol) in dry acetonitrile (20 mL) at 50° C. under a nitrogen atmosphere. After the addition the reaction mixture was stirred for an additional 2 hours at 50° C. and cooled to room temperature. The solid which formed was filtered and recrystallized from acetonitrile to provide the title product as a light yellow colored solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06958141B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-4ab0b8a1598c4553ba700521b0b53c5c |
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| Source note | uspto-grants-2005_10 |
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