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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28002생성일: 2026년 10월 24일

3-(N-carbethoxymethyl-N-methylsulfamoyl)-thiophene-2-carboxylic acid methyl ester → 2H-Thieno(2,3-e)-1,2-thiazine-3-carboxylic acid, 4-hydroxy-2-methyl-, methyl ester, 1,1-dioxide

https://huagongshe.com/ko/reaction/28002

반응식

참여 물질

역할이름HCID투입량
반응물3-(N-carbethoxymethyl-N-methylsulfamoyl)-thiophene-2-carboxylic acid methyl esterHCID 2808794—
반응물Sodium MethoxideHCID 10942334—
생성물2H-Thieno(2,3-e)-1,2-thiazine-3-carboxylic acid, 4-hydroxy-2-methyl-, methyl ester, 1,1-dioxideHCID 54690599—

반응 단계

13.2 G. of 3-(N-carbethoxymethyl-N-methyl-sulfamoyl)-thiophene-2-carboxylic acid methyl ester are suspended in 42 ml. of a 1-N methanolic sodium methylate solution in the cold and under a nitrogen stream. After stirring for 15 minutes, a clear solution results. The solution is heated to reflux for 20 minutes, then cooled, neutralized and evaporated in vacuo. The residue is taken up in methylene chloride, shaken once each time with water and a sodium bicarbonate solution, dried and evaporated. The residue is brought to crystallization with methanol. There is obtained 3-carbomethoxy-4-hydroxy-2-methyl-2H-thieno[2,3-e]-1,2-thiazine 1,1-dioxide of melting point 193°-195° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04224445
출처 데이터셋uspto-grants-1980_09
ORD IDord-b01677b1b0d646c1a124aeae98ac5e78
출처 메모uspto-grants-1980_09