Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 516911생성일: 2026년 10월 27일
Diethyl squarate → 6-chloro-3-(2-ethoxy-3,4-dioxo-cyclobut-1-enylamino)-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide
https://huagongshe.com/reaction/516911
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Diethyl squarate | HCID 123228 | — |
| 반응물 | 3-Amino-6-chloro-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide | HCID 18373483 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 6-chloro-3-(2-ethoxy-3,4-dioxo-cyclobut-1-enylamino)-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide | HCID 56844293 | — |
반응 단계
A solution of 3,4-diethoxy-3-cyclobutene-1,2-dione (2.83 g, 1.2 equiv) in ethanol (30 ml) was treated with TEA (1.54 g, 1.1 equiv) and the reaction mixture was heated to 45° C. 3-Amino-6-chloro-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide (3.7 g, 1 equiv) was added portion wise over 30 minutes, with vigorous stirring, maintaining the reaction mixture at 45° C. The reaction mixture was stirred at 45° C. for 1 hour and then allowed to cool to RT. The solvent was removed in vacuo and the residue was partitioned between EtOAc (600 ml) and water (2×200 ml). The aqueous portion was separated and extracted with EtOAc (3×200 ml) and the combined organic extracts were washed with water (3×200 ml) and allowed to stand over night. The resulting solid was collected by filtration and dried in vacuo to afford the title compound. The mother liquor was evaporated to give a yellow/brown oily solid which was triturated with ethanol (100 ml). The solid was collected by fitration, washed with EtOH and dried in vacuo to afford the title compound; [M+H]+ 390.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09115087B2 |
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| 출처 데이터셋 | uspto-grants-2015_08 |
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| ORD ID | ord-8d6acff6407349bdaa2d721c125b638b |
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| 출처 메모 | uspto-grants-2015_08 |
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