関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Amino-6-methoxy-3-nitropyridine | HCID 3852428 | — |
| 反応物 | 6-Bromo-3-nitro-2-pyridinamine | HCID 12097745 | — |
| 溶媒 | Acetic Acid Mixture with Hydrobromic Acid | HCID 21893785 | — |
| 生成物 | HCID 178419698 | HCID 178419698 | 95% |
反応手順
6-Bromo-3-nitro-pyridin-2-ylamine. To a glass pressure vessel containing 6-methoxy-3-nitro-pyridin-2-ylamine (5.0 g, 29.5 mmol) was added 30% hydrogen bromide/acetic acid (60 mL). The vessel was sealed, and the contents were heated to 60° C. for 24 h. The reaction mixture was cooled, and the solvent was removed in vacuo giving 6.8 g (>95%) of crude 6-amino-5-nitro-pyridin-2-ol hydrobromide (HPLC: Rt=5.46). This material (2.0 g, 8.5 mmol) was taken up in toluene (30 mL), followed by phosphorus pentoxide (2.4 g, 17.0 mmol) and tetrabutyl ammonium bromide (3.2 g, 9.7 mmol). The mixture was heated to reflux for 4 h. The reaction mixture was cooled to 0° C., diluted with saturated NaHCO3, and extracted with ethyl acetate (3×100 mL). The combined organics were washed with water (100 mL) and dried (Na2SO4) to afford 1.18 g (64%) of 6-bromo-3-nitro-pyridin-2-ylamine.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07271261B2 |
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| 出典データセット | uspto-grants-2007_09 |
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| ORD ID | ord-ef282a0871e9489fae960e26493665f9 |
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| 出典メモ | uspto-grants-2007_09 |
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