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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

反応式

関与物質

役割名称HCID仕込み量
反応物Piracetam hydrazideHCID 3565593—
反応物Sodium MethoxideHCID 10942334—
反応物ethoxy[3-(4fluorophenyl)(1H-indazol-5-yl)]methanimine hydrochlorideHCID 22479739—
溶媒MethanolHCID 887—
生成物1-({3-[3-(4-Fluorophenyl)-1H-Indazol-5-Yl]-1H-1,2,4-Triazol-5-Yl}Methyl)Pyrrolidine-2-OneHCID 2248025634%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07220771B2
出典データセットuspto-grants-2007_05
ORD IDord-f80f1a056ce442a9a847f5fd42749348
出典メモuspto-grants-2007_05