Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,3-Dichloroacetone | HCID 10793 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 136354634 | HCID 136354634 | — |
| Product | HCID 12369474 | HCID 12369474 | — |
| Product | HCID 136354633 | HCID 136354633 | — |
Reaction Steps
The 2-thiocarbamyl compounds from Example 1 (0.27 mole) and 1,3-dichloroacetone (0.55 mole) in dioxan (55 ml.) were stirred and heated at 130° C. for 2 hours. The mixture was poured into water, the resultant precipitate washed with hot water and dried to yield 2-(1-methyl-5-nitroimidazol-2-yl)-4-chloromethylthiazole m.p. 160°-2° C. and 2-(1-p-toluenesulphonyloxyethyl-5-nitroimidazol-2-yl)-4-chloromethylthiazole respectively. The 1-p-toluenesulphonyloxy compound, on treatment as described at the end of Example 2, yielded 2-(1-vinyl-5-nitroimidazol-2-yl)-4-chloromethylthiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03989690 |
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| Source dataset | uspto-grants-1976_11 |
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| ORD ID | ord-12af5ba4d6f3469f8e4025006c77b437 |
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| Source note | uspto-grants-1976_11 |
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