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HRID 466255作成日:2026年10月24日

Methanesulfonamide, N-(aminosulfonyl)-N-methyl- → 1-[(N-Methylsulfonyl-N-methylamino)sulfonyl]-3-(4-methoxy-6-methyl-2-pyrimidyl)urea

https://huagongshe.com/ja/reaction/466255

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonamide, N-(aminosulfonyl)-N-methyl-HCID 11084607—
反応物Phenyl (4-methoxy-6-methylpyrimidin-2-yl)carbamateHCID 13577349—
溶媒ChlorobenzeneHCID 7964—
生成物1-[(N-Methylsulfonyl-N-methylamino)sulfonyl]-3-(4-methoxy-6-methyl-2-pyrimidyl)ureaHCID 1337178396.4%

反応条件

温度100 °C

反応手順

37.6 g of (N-methylsulfonyl-N-methylamino)sulfonamide are dissolved in 500 ml of chlorobenzene, 51.8 g of phenyl 4-methoxy-6-methyl-2-pyrimidylcarbamate are added dropwise at room temperature to the solution, and the mixture is stirred for 5 hours at 100° C. The mixture is cooled to 0° C., the precipitate is then filtered off, and, after washing with 100 ml of chlorobenzene, 68.8 g of the desired product of a purity of 98.7% are obtained. This corresponds to a yield of 96.4% of theory. The melting point of the product is 118-120° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05155222
出典データセットuspto-grants-1992_10
ORD IDord-55bb1e8f570f42b7b39a2ad831b1a37b
出典メモuspto-grants-1992_10