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N-bromobutanimide → (5-Bromopyrazin-2-yl)-(6-trifluoromethyl-pyridin-3-yl)-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | Pyrazin-2-yl-(6-trifluoromethyl-pyridin-3-yl)-amine | HCID 66615925 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | (5-Bromopyrazin-2-yl)-(6-trifluoromethyl-pyridin-3-yl)-amine | HCID 86634697 | — |
反応手順
A solution of pyrazin-2-yl-(6-trifluoromethyl-pyridin-3-yl)-amine (0.47 g) was dissolved in 50 Ml MeOH and then charged with N-bromosuccinimide (0.35 g) in a single portion as a solid. The reaction was stirred overnight at room temperature, then concentrated in vacuo. Purification by silica gel chromatography (25% EtOAc in hexanes) afforded the title compound: 1H NMR (400 MHz, CHLOROFORM-D) δ ppm 6.7 (s, 1H) 7.5 (s, 1H) 7.9 (s, 1H) 8.2 (s, 2H) 8.6 (s, 1H); (M+H)+320.9.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08835451B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-e92bde82a09e49dcb5bab65f5540dada |
| 出典メモ | uspto-grants-2014_09 |