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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1454927생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1454927

반응식

참여 물질

역할이름HCID투입량
반응물2-Mesitylenesulfonyl chlorideHCID 13046—
반응물Sodium hydrideHCID 24758—
반응물Indazole-3-carboxylic acidHCID 78250—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물1-(2,4,6-Trimethylbenzenesulphonyl)-1H-indazole-3-carboxylic acidHCID 12106070—

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07482342B2
출처 데이터셋uspto-grants-2009_01
ORD IDord-71a6a69b58b34eba9167559fac26177c
출처 메모uspto-grants-2009_01