関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 5-Chloropyrrolo[2,1-f][1,2,4]triazin-4(1H)-one | HCID 135742086 | — |
| 反応物 | HCID 178479710 | HCID 178479710 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 4,5-Dichloropyrrolo[2,1-f][1,2,4]triazine | HCID 21081669 | 67.3% |
反応手順
To a solution of 5-chloropyrrolo[2,1-f][1,2,4]triazin-4(3H)-one (5.00 g, 29.5 mmol) in toluene (100 mL) at rt under nitrogen was added diisopropylethylamine (5.14 mL, 29.5 mmol) followed by phosphorus(III) oxychloride (8.25 mL, 88.5 mmol). The mixture was heated at 100° C. for 20 h and was then cooled to rt. The reaction was slowly added to saturated aqueous sodium bicarbonate solution (500 mL) at 0° C. After the addition was complete, the mixture was stirred at rt for 30 min. The aqueous phase was extracted with ethyl acetate (3×500 mL), dried over anhydrous MgSO4, and concentrated in vacuo to give the crude product (3.73 g, 67%) as a yellow solid which was used without further purification. 1H NMR (CDCl3) δ 8.03 (s, 1H), 7.70 (d, 1H, J=2.8 Hz), 6.84 (d, 1H, J=2.8 Hz); MS(ESI+) m/z 188.1 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07439246B2 |
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| 出典データセット | uspto-grants-2008_10 |
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| ORD ID | ord-eef68dead9064969a4b2d1a50ede38cd |
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| 出典メモ | uspto-grants-2008_10 |
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