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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 236534생성일: 2026년 10월 25일

2-Amino-4-methoxy-6-methyl-1,3,5-triazine → N-[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-4-nitrothiophene-2-sulfonamide

https://huagongshe.com/reaction/236534

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-4-methoxy-6-methyl-1,3,5-triazineHCID 15466—
반응물4-Nitrothiophene-2-sulfonyl isocyanateHCID 20215702—
용매AcetonitrileHCID 6342—
생성물N-[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-4-nitrothiophene-2-sulfonamideHCID 13472988—

반응 단계

To 1.4 g of 2-amino-4-methoxy-6-methyl-1,3,5-triazine suspended in 25 ml of anhydrous acetonitrile with stirring at ambient temperature was added 2.4 g of 4-nitrothiophene-2-sulfonyl isocyanate. After stirring for sixteen hours at ambient temperature, the product which was present as a precipitate was removed by filtration and washed with 1-chlorobutane. It melted at 188° with decomposition and showed infrared absorption spectrum peaks at 1740, 1600 and 1560 cm-1 consistent for the desired aminocarbonylsulfonamide structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04645529
출처 데이터셋uspto-grants-1987_02
ORD IDord-a885e71857244ac1afb803c6848aafc2
출처 메모uspto-grants-1987_02