참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Methylpyridine | HCID 7975 | — |
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | Chlorosulfonic acid | HCID 24638 | — |
| 반응물 | Benzenamine, 4-(2-benzothiazolyl)-2-iodo- | HCID 384526 | — |
| 생성물 | Sodium 4-(benzothiazol-2-yl)phenylsulphamate | HCID 23717892 | — |
반응 단계
To anhydrous 2-picoline (1.05 g, 11 mmol) was slowly added dropwise chlorsulphonic acid (0.26 g, 2.21 mmol) below 10° C. then 2-(4'-amino-3'-iodophenyl)benzothiazole (0.5 g, 2.21 mmol). The mixture was heated to 50° C. with stirring for 1 hour. After leaving to stand for 2 hours at room temperature, 6 ml of 10% aqueous sodium carbonate was added. The resulting mixture was stirred for 40 minutes at room temperature and concentrated under reduced pressure. The precipitate was filtered off, washed carefully with cold water and treated with hot chlorform. Golden crystals were afforded (0.62 g, 85.5%), m.p. 288-290° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06034246 |
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| 출처 데이터셋 | uspto-grants-2000_03 |
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| ORD ID | ord-238ae6d3d5b64f388881ec0f478e52b2 |
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| 출처 메모 | uspto-grants-2000_03 |
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