戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1248388作成日:2026年10月25日

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/1248388

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-4-methoxy-6-methyl-1,3,5-triazineHCID 15466—
反応物4-Nitrothiophene-2-sulfonyl isocyanateHCID 20215702—
溶媒AcetonitrileHCID 6342—
生成物N-[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-4-nitrothiophene-2-sulfonamideHCID 13472988—

反応手順

To 1.4 g of 2-amino-4methoxy-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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04523943
出典データセットuspto-grants-1985_06
ORD IDord-b6c0a213d1df42a18e99e4c9f2ebec93
出典メモuspto-grants-1985_06