Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 619044생성일: 2026년 10월 26일
Hydrochloric Acid → 5-tert-Butyl-thiophene-2-sulfonic acid [4-(3-nitro-phenyl)-thiazol-2-yl]-amide
https://huagongshe.com/reaction/619044
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 4-(3-Nitro-phenyl)-thiazol-2-ylamine hydrobromide | HCID 2870445 | — |
| 반응물 | 5-Tert-butylthiophene-2-sulfonyl chloride | HCID 21845564 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | 5-tert-Butyl-thiophene-2-sulfonic acid [4-(3-nitro-phenyl)-thiazol-2-yl]-amide | HCID 86753755 | — |
반응 단계
A mixture of 0.5 g of 4-(3-nitro-phenyl)-thiazol-2-ylamine hydrobromide with 0.43 g of 5-tert-butyl-thiophene-2-sulfonyl chloride was stirred overnight with 2 ml of pyridine. The resulting, red colored suspension was poured into 30 ml of 1N hydrochloric acid and the mixture was extracted three times with 30 ml of ethyl acetate each time. The organic phases were combined, dried with magnesium sulphate and the solvent was removed on a rotary evaporator. The residue was chromatographed on 50 g of Kieselgel 60 with ethyl acetate/hexane (1:2) as the eluent. The product-containing fractions were concentrated and the residue was dissolved in a mixture of 20 ml of ethanol and 20 ml of 2N sodium hydroxide solution. After the addition of 0.4 g of active charcoal the mixture was stirred at room temperature for 30 minutes and subsequently the active charcoal was filtered off. 0.20 g of 5-tert-butyl-thiophene-2-sulfonic acid [4-(3-nitro-phenyl)-thiazol-2-yl]-amide separated as yellowish crystals after neutralization with concentrated hydrochloric acid and repeated boiling.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05958910 |
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| 출처 데이터셋 | uspto-grants-1999_09 |
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| ORD ID | ord-ce3afca5fad3405fa923234338b859db |
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| 출처 메모 | uspto-grants-1999_09 |
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