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1,2,3,6-Tetrahydrophthalimide → N-[2-(2-methyl-5-nitro-1-imidazolyl)ethyl]-1,2,3,6-tetrahydrophthalimide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,2,3,6-Tetrahydrophthalimide | HCID 6808 | — |
| 反応物 | Potassium | HCID 5462222 | — |
| 反応物 | 1-(2-Hydroxyethyl)-2-methyl-5-nitroimidazole tosylate | HCID 86734258 | — |
| 生成物 | N-[2-(2-methyl-5-nitro-1-imidazolyl)ethyl]-1,2,3,6-tetrahydrophthalimide | HCID 21491658 | — |
反応手順
1,2,3,6-Tetrahydrophthalimide 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 obtained is concentrated and the concentrate distributed between water and toluene. The toluene layer is separated and the solvent is evaporated to leave a residue which is recrystallized from 2-propanol, affording N-[2-(2-methyl-5-nitro-1-imidazolyl)ethyl]-1,2,3,6-tetrahydrophthalimide melting at about 118°-123° 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-90b718b0ea0140c8a9bcde1fb2cba8b1 |
| 出典メモ | uspto-grants-1976_12 |