反応式
[Cl:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([NH2:8])[CH:3]=1.[I:9]N1C(=O)CCC1=O>C(O)(=O)C>[Cl:1][C:2]1[C:7]([I:9])=[CH:6][N:5]=[C:4]([NH2:8])[CH:3]=1参加物
反応条件
- 温度
- 80 °C
実験手順
4-Chloropyridin-2-amine (0.142 g, 1.10 mmol) and N-iodosuccinimide (0.273 g, 1.22 mmol) were combined in 1.5 mL of acetic acid. The solution was sonicated briefly and then heated to 80° C. After 1 hour the solution was cooled to room temperature and then concentrated under vacuum. After adjusting the pH to ˜ 8/9 with aqueous ammonia, a light brown solid was collected by filtration. The solid was purified on a 12 g Combiflash column eluting with a gradient of DCM to 5% methanol/0.25% NH4OH (˜28% in water)/DCM. The fractions containing the product were combined and concentrated under vacuum to give 4-chloro-5-iodopyridin-2-amine (187 mg, 67%) as an off-white solid. 1H NMR (500 MHz, DMSO-d6) δ ppm 8.20 (1 H, s), 6.69 (1 H, s), 6.40 (2 H, s); LCMS-ESI (POS), M/Z, M+1: Found 254.9.
後処理
- customThe solution was sonicated briefly
- temperatureAfter 1 hour the solution was cooled to room temperature
- concentrationconcentrated under vacuum
- filtrationa light brown solid was collected by filtration
- customThe solid was purified on a 12 g Combiflash column
- washeluting with a gradient of DCM to 5% methanol/0.25% NH4OH (˜28% in water)/DCM
- additionThe fractions containing the product
- concentrationconcentrated under vacuum
出典と根拠
- ORDレコード
- ord-d790b5766a0d4515905ce822406577a5
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08841312B2
関連ノート
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