化工社化工社 化学情報印刷レポート · 研究参考用
Isopropanol → (1-Methylethyl) [3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]phenyl]carbamate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Isopropanol | HCID 3776 | — |
| 反応物 | 4-Methoxy-6-methylpyrimidin-2-amine | HCID 587236 | — |
| 反応物 | m-Isocyanatobenzenesulfonyl isocyanate | HCID 13138205 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (1-Methylethyl) [3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]phenyl]carbamate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04225337 |
| 出典データセット | uspto-grants-1980_09 |
| ORD ID | ord-117ab8697f8f439cae2eb0a9f17a5622 |
| 出典メモ | uspto-grants-1980_09 |