참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Chlorosulfonic acid | HCID 24638 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 1-(Methylsulfonyl)-1H-Benzimidazol-2-Amine | HCID 22997045 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | N-methanesulfonyl-5-chlorosulfonyl-2-aminobenzimidazole | HCID 22997216 | — |
반응 단계
To 9.5 mL (20 eq., 142 mmol) of well stirred chlorosulfonic acid at ˜25° C. was added N-methanesulfonyl-2-aminobenzimidazole (1.5 g, 7.1 mmol) in small portions over 1C minutes with slight exotherming. The solution was stirred at ˜25° C. for 3.5 hours, then was added dropwise to a well stirred mixture of ice and water. The aqueous solution was slowly basified to pH ˜7.5 with solid sodium bicarbonate and extracted with EtOAc. A precipitate formed in the organic phase which was filtered off and was washed with H20 and dried on the filter to yield 1.23 g of N-methanesulfonyl-5-chlorosulfonyl-2-aminobenzimidazole. HPLC, single peak, ret. time=7.61 min. MS: Obs. M +H@ 310.0 amu.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06613743B2 |
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| 출처 데이터셋 | uspto-grants-2003_09 |
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| ORD ID | ord-4e5339decb32429eadc0cf684119054e |
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| 출처 메모 | uspto-grants-2003_09 |
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