Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylimidazole | HCID 1390 | — |
| Reactant | HCID 86632117 | HCID 86632117 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86632115 | HCID 86632115 | 80.1% |
Reaction Steps
0.5 g N-(2-bromoethyl)-4-[(4,5-dimethyl-1,3-thiazol-2-yl)diazenyl]-N-ethylaniline is dissolved in 10 ml acetonitrile followed by subsequent addition of 5.3 g 1-methyl-1H-imidazole. The reaction mixture is heated at 80° C. overnight. After cooling to room temperature, the formed precipitate is filtered off, washed with acetonitrile, and dried under vacuum at 40° C. 0.49 g of 1-{2-[{4-[(4,5-dimethyl-1,3-thiazol-2-yl)diazenyl]phenyl}(ethyl)amino]ethyl}-3-methyl-1H-imidazol-3-ium bromide are obtained as a red crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07658770B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-2416fea2647347ef9af2e988c079c0ae |
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| Source note | uspto-grants-2010_02 |
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