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HRID 1353888作成日:2026年10月25日
Piracetam hydrazide → 1-({3-[3-(4-Fluorophenyl)-1H-Indazol-5-Yl]-1H-1,2,4-Triazol-5-Yl}Methyl)Pyrrolidine-2-One
https://huagongshe.com/reaction/1353888
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Piracetam hydrazide | HCID 3565593 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 反応物 | ethoxy[3-(4fluorophenyl)(1H-indazol-5-yl)]methanimine hydrochloride | HCID 22479739 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 1-({3-[3-(4-Fluorophenyl)-1H-Indazol-5-Yl]-1H-1,2,4-Triazol-5-Yl}Methyl)Pyrrolidine-2-One | HCID 22480256 | 34% |
反応手順
A suspension of ethoxy[3-(4-fluorophenyl)(1H-indazol-5-yl)]methanimine hydrochloride (0.300 g, 0.94 mmol) and N-amino-2-(2-oxopyrrolidinyl)acetamide (0.442 g, 2.81 mmol) in 4 mL of anhydrous methanol was prepared. An excess of a commercial solution of sodium methoxide in methanol (0.643 mL, 4.37 M) was added. Upon adding the basic solution, the reaction mixture became clear then cloudy. After an hour, the temperature was raised to reflux temperature and was maintained for 48 hours. The reaction was then quenched with water, the pH adjusted to neutral and the crude product extracted with ethyl acetate. The title compound was purified by preparative HPLC (0.118 g, 34% yield): 1H NMR (CD3OD) δ 8.68 (s, 1H), 8.07–8.02 (m, 3H), 7.68 (d, 1H), 7.29 (t, 2H), 4.66 (s, 2H), 3.53 (t, 2H), 2.47 (t, 2H), 2.10 (quintet, 2H); ES-MS (m/z) 377 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07220771B2 |
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| 出典データセット | uspto-grants-2007_05 |
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| ORD ID | ord-f80f1a056ce442a9a847f5fd42749348 |
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| 出典メモ | uspto-grants-2007_05 |
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