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HRID 28047作成日:2026年10月24日

Isopropanol → (1-Methylethyl) [3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]phenyl]carbamate

https://huagongshe.com/ja/reaction/28047

反応式

関与物質

役割名称HCID仕込み量
反応物IsopropanolHCID 3776—
反応物4-Methoxy-6-methylpyrimidin-2-amineHCID 587236—
反応物m-Isocyanatobenzenesulfonyl isocyanateHCID 13138205—
溶媒DichloromethaneHCID 6344—
生成物(1-Methylethyl) [3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]phenyl]carbamateHCID 13138206—

反応手順

To an anhydrous solutiion o 2.3 g of m-isocyanatobenzenesulfonyl isocyanate in 50 ml of methylene chloride was added in small portions 1.4 g of 2-amino-4-methoxy-6-methylpyrimidine. Efficient stirring was maintained during the addition and for three additional hours. The intermediate thus obtained, 3-isocyanato-N-[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]benenesulfonamide, was reacted further by adding one gram of 2-propanol and stirring the resultant mixture for an additional sixteen hours. Filtration of the reaction mixture and evaporation of the filtrate yielded the desired product melting at 173°-180°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04225337
出典データセットuspto-grants-1980_09
ORD IDord-117ab8697f8f439cae2eb0a9f17a5622
出典メモuspto-grants-1980_09