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Chloroform → 2,6-Dichloro-3-iodoimidazo[1,2-a]pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Chloroform | HCID 6212 | — |
| 反応物 | N-Iodosuccinimide | HCID 120273 | — |
| 反応物 | 2,6-Dichloroimidazo[1,2-A]pyridine | HCID 11769257 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 2,6-Dichloro-3-iodoimidazo[1,2-a]pyridine | HCID 11141504 | 80% |
反応手順
To a suspension of 2,6-dichloro-imidazo[1,2-a]pyridine, compound 12 (4.0 g, 0.02 mol) in dry CH3CN (50 mL) was added N-iodosuccinimide (NIS, 5.3 g, 0.024 mol) and the mixture stirred at room temperature for 1 h. The reaction mixture was heated at reflux for 10 min and then cooled to room temperature. Chloroform (200 mL) was added to the reaction mixture and the organic phase washed successively with 10% NaOH (100 mL), sodium thiosulfate (100 mL) and water (2×100 mL) then dried over magnesium sulfate, filtered and concentrated to dryness under reduced pressure. The resulting solid was suspended in MeOH and filtered to give 5.0 g (80%) of compound 19 as white crystalline solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06214801B1 |
| 出典データセット | uspto-grants-2001_04 |
| ORD ID | ord-9c68069183404c3992bec70627490fa6 |
| 出典メモ | uspto-grants-2001_04 |