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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Mesitylenesulfonyl chloride | HCID 13046 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Indazole-3-carboxylic acid | HCID 78250 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-(2,4,6-Trimethylbenzenesulphonyl)-1H-indazole-3-carboxylic acid | HCID 12106070 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07482342B2 |
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| 출처 데이터셋 | uspto-grants-2009_01 |
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| ORD ID | ord-71a6a69b58b34eba9167559fac26177c |
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| 출처 메모 | uspto-grants-2009_01 |
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