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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

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl squarateHCID 123228—
반응물3-Amino-6-chloro-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamideHCID 18373483—
용매EthanolHCID 702—
생성물6-chloro-3-(2-ethoxy-3,4-dioxo-cyclobut-1-enylamino)-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamideHCID 56844293—

반응 조건

온도45 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09115087B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-8d6acff6407349bdaa2d721c125b638b
출처 메모uspto-grants-2015_08