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HRID 22656作成日:2026年10月24日

Acetic Anhydride → Methyl 1-acetyl-1H-indazole-5-carboxylate

https://huagongshe.com/ja/reaction/22656

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物Pentyl nitriteHCID 10026—
反応物18-Crown-6HCID 28557—
反応物Potassium AcetateHCID 517044—
反応物Methyl 4-amino-3-methylbenzoateHCID 2736799—
溶媒ChloroformHCID 6212—
生成物Methyl 1-acetyl-1H-indazole-5-carboxylateHCID 2259133247.4%

反応手順

To a stirred mixture of methyl 3-methyl-4-aminobenzoate (5.0 g, 30.0 mmol) and potassium acetate (2.94 g, 30.0 mmol) in chloroform (50 mL) is added acetic anhydride (5.66 mL, 60.0 mmol). The mixture is stirred for 30 min at rt, followed by the addition of 18-crown-6 (1.58 g, 6.0 mmol) and n-amyl nitrite (7.78 g, 66.0 mmol). The mixture is heated to reflux for 16 h, followed by cooling to rt. The mixture is washed sequentially with aqueous sodium bicarbonate solution (2×), water and brine. The organic layer is dried over MgSO4, filtered and concentrated in vacuo. The crude product is purified by flash chromatography on silica gel. Elution with hexanes-EtOAc (80:20) gives 3.1 g (47%) of methyl 1-acetyl-1H-indazole-5-carboxylate as a yellow solid: 1H NMR (400 MHz, CDCl3) δ 8.52-8.50, 8.3, 8.2, 4.0, 2.8.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06849620B2
出典データセットuspto-grants-2005_02
ORD IDord-6062662749034ec397236ef61309513e
出典メモuspto-grants-2005_02