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Potassium → N-[2-(2-methyl-5-nitro-1-imidazolyl)ethyl]-acenaphthene-1,2-dicarboximide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium | HCID 5462222 | — |
| 反応物 | Acenaphthene-1,2-dicarboximide | HCID 21491653 | — |
| 反応物 | 1-(2-Hydroxyethyl)-2-methyl-5-nitroimidazole tosylate | HCID 86734258 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | N-[2-(2-methyl-5-nitro-1-imidazolyl)ethyl]-acenaphthene-1,2-dicarboximide | HCID 21491671 | — |
反応手順
Acenaphthene-1,2-dicarboximide is converted to the potassium salt and reacted with 1-(2-hydroxyethyl)-2-methyl-5-nitroimidazole tosylate according to the procedure described in Example 13. The crude reaction mixture is cooled and diluted with water, and then extracted with toluene. The solvent is evaporated from the toluene extract and the residue recrystallized from ethanol to give N-[2-(2-methyl-5-nitro-1-imidazolyl)ethyl]-acenaphthene-1,2-dicarboximide melting at about 183°-185° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US03997572 |
| 出典データセット | uspto-grants-1976_12 |
| ORD ID | ord-89f21b68d4a7411f94b4a050c9f0a229 |
| 出典メモ | uspto-grants-1976_12 |