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HRID 1454927作成日:2026年10月26日

2-Mesitylenesulfonyl chloride → 1-(2,4,6-Trimethylbenzenesulphonyl)-1H-indazole-3-carboxylic acid

https://huagongshe.com/reaction/1454927

反応式

関与物質

役割名称HCID仕込み量
反応物2-Mesitylenesulfonyl chlorideHCID 13046—
反応物Sodium hydrideHCID 24758—
反応物Indazole-3-carboxylic acidHCID 78250—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物1-(2,4,6-Trimethylbenzenesulphonyl)-1H-indazole-3-carboxylic acidHCID 12106070—

反応条件

温度0 °C

反応手順

NaH (60% in oil, 40 mmol) is washed under argon with petroleum ether and then suspended in 60 ml of anhydrous DMF. An indazole-3-carboxylic acid solution (3.35 g, 20 mmol) in anhydrous DMF (50 ml) is added dropwise to this suspension kept at 0° C. The reaction mixture becomes clear. When the addition is complete, the medium is allowed to react for 30 min at room temperature and then the reaction mixture is again cooled to 0° C. Mesitylenesulphonyl chloride (4.82 g, 22 mmol) in solution in anhydrous tetrahydrofuran (THF) (50 ml) is added. The ice bath is removed and a suspension appears. The medium is allowed to react for 30 min at room temperature. The solvents are evaporated under vacuum and the residue is taken up in 0.1N NaOH solution. The solution obtained is washed with diethyl ether and then acidified with 6N HCl. The compound which separates is filtered, and taken up in AcOEt. The AcOEt solution is dried over Na2SO4 and then evaporated. The residue (6.18 g) is recrystallized from AcOEt/petroleum ether.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07482342B2
出典データセットuspto-grants-2009_01
ORD IDord-71a6a69b58b34eba9167559fac26177c
出典メモuspto-grants-2009_01