참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Hydrogen Peroxide | HCID 784 | — |
| 반응물 | Sodium Thiosulfate | HCID 24477 | — |
| 반응물 | Potassium Permanganate | HCID 516875 | — |
| 반응물 | 5-Chloro-2-(methylthio)benzothiazole | HCID 645746 | — |
| 생성물 | 5-Chloro-2-(methylsulfonyl)benzo[d]thiazole | HCID 21985716 | 100% |
반응 단계
A mixture of 1.80 g (8.34 mmols) of 5-chloro-2-methylthiobenzothiazole, 1.80 g (11.39 mmols) of potassium permanganate and 45 ml of 50% aqueous acetic acid solution was stirred at room temperature for an hour. After the reaction, a 30.0 to 35.5% aqueous hydrogen peroxide solution was dropwise added to the mixture with stirring under ice cooling until to be colorless. An aqueous sodium thiosulfate was added to the mixture followed by extraction of the solution with chloroform. The chloroform layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to afford 2.05 g (yield: 100%) of 5-chloro-2-methanesulfonylbenzothiazole. A mixture of 1.64 g (6.62 mmols) of the above compound, 2.57 g (9.91 mmols) of Compound b obtained in Reference Example 2 and 40 ml of acetonitrile was heated under reflux for 20 hours. The mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: chloroform/methanol =100/1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05053408 |
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| 출처 데이터셋 | uspto-grants-1991_10 |
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| ORD ID | ord-e85f73c011aa41a6a1003f561526603f |
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| 출처 메모 | uspto-grants-1991_10 |
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