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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 595668생성일: 2026년 10월 24일

Ethyl 1-propenyl ether → 5-bromo-2-(5-ethoxy-4-methyl-4,5-dihydroisoxazol-3-yl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide

https://huagongshe.com/ko/reaction/595668

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 1-propenyl etherHCID 13570—
반응물Sodium BicarbonateHCID 516892—
반응물5-bromo-N-hydroxy-3-(methylcarbamoyl)-6-(N-methylmethylsulfonamido)benzofuran-2-carbimidoyl chlorideHCID 90332447—
용매DimethylformamideHCID 6228—
생성물5-bromo-2-(5-ethoxy-4-methyl-4,5-dihydroisoxazol-3-yl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamideHCID 9033242183.3%

반응 단계

A mixture of 5-bromo-N-hydroxy-3-(methylcarbamoyl)-6-(N-methylmethylsulfonamido)benzofuran-2-carbimidoyl chloride (400 mg, 0.91 mmol), 1-ethoxyprop-1-ene (392 mg, 4.56 mmol) and NaHCO3 (153 mg, 1.82 mmol) in DMF (10 mL) was stirred at room temperature for 16 h. It was concentrated, diluted with water, extracted with EtOAc, the organic layers were washed with brine, dried over Na2SO4, and concentrated. The residue was purified by column chromatography (PE:EA=2:1) to get product 5-bromo-2-(5-ethoxy-4-methyl-4,5-dihydroisoxazol-3-yl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide (370 mg, yield: 83%). MS (M+H)+: 488/490.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09243002B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-ade4085fa6194ffaae10b313b720147a
출처 메모uspto-grants-2016_01