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HRID 915746作成日:2026年10月27日
2-(Methylamino)ethanol → Benzyl (S)-2-[6-hydroxy-7-[(2-hydroxyethyl)methylamino]-1H-indazol-1-yl]-1-methylethylcarbamate
https://huagongshe.com/reaction/915746
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-(Methylamino)ethanol | HCID 8016 | — |
| 反応物 | Benzyl 2-(7-bromo-6-hydroxy-1H-indazol-1-yl)-1-methylethylcarbamate | HCID 136338690 | — |
| 溶媒 | Ammonium Chloride | HCID 25517 | — |
| 生成物 | Benzyl (S)-2-[6-hydroxy-7-[(2-hydroxyethyl)methylamino]-1H-indazol-1-yl]-1-methylethylcarbamate | HCID 136375621 | 68% |
反応手順
To a stirred solution of the product from Step A (0.24 g, 0.59 mmol) was added 2-(methyamino)ethanol (2.0 mL) and the solution was heated at 80° C. for 18 h. A saturated aqueous solution of ammonium chloride (20 mL) was added to the reaction mixture, which was extracted with ethyl acetate (3×50 mL). The combined extracts were washed with brine (10 mL), dried (MgSO4) and evaporated to give a residue which was purified by chromatography (silica, 30% ethyl acetate in hexane) to give an oil (0.16 g, 68%): 1H NMR (CDCl3) δ 8.50 (1H, brs), 8.01 (1H, s), 7.30 (6H, m), 6.77 (1H, d, J=8.4 Hz), 5.02 (2H, m), 4.59 (2H, m), 4.77 (1H, brs), 4.09 (1H, m), 3.69 (1H, m), 3.36 (2H, m), 2.93 (3H, s), 1.26 (3H, d, J=6.4 Hz); MS (ES) m/z 399 (M+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07268131B2 |
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| 出典データセット | uspto-grants-2007_09 |
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| ORD ID | ord-bf0826c99f774a3c819f5b0963c970a3 |
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| 出典メモ | uspto-grants-2007_09 |
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