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Sodium Iodide → 1-Thioacetylmethyl-2-nitroimidazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Iodide | HCID 5238 | — |
| 反応物 | 2-Nitroimidazole | HCID 10701 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Chloromethylthioacetate | HCID 53833355 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 1-Thioacetylmethyl-2-nitroimidazole | HCID 86656269 | — |
反応手順
To a solution of the chloromethylthioacetate in MeCN (100 mL) was added 2-nitroimidazole (3 g), NaI (1 g) and diisopropylethyl amine (DIEA) and refluxed. A precipitate formed after 3 h. Additional DIEA (3 mL) was added to the reaction mixture and refluxed for 4 h. Volatiles were removed, EtOAc (300 mL) added to the residue, and the ensuing mixture filtered. The filtrate was washed with water, 1M aqueous citric acid, brine, and concentrated to yield a residue. The residue was separated by column chromatography using 0-90% EtOAc/Hexane as eluent to yield 1-thioacetylmethyl-2-nitroimidazole (vi, 3.15 g) that was chlorinated as described above in Example 1A to yield compound vii.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08309554B2 |
| 出典データセット | uspto-grants-2012_11 |
| ORD ID | ord-8296122d7f0340a3a24c6d0c5a488814 |
| 出典メモ | uspto-grants-2012_11 |