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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 466255생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonamide, N-(aminosulfonyl)-N-methyl-HCID 11084607—
반응물Phenyl (4-methoxy-6-methylpyrimidin-2-yl)carbamateHCID 13577349—
용매ChlorobenzeneHCID 7964—
생성물1-[(N-Methylsulfonyl-N-methylamino)sulfonyl]-3-(4-methoxy-6-methyl-2-pyrimidyl)ureaHCID 1337178396.4%

반응 조건

온도100 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05155222
출처 데이터셋uspto-grants-1992_10
ORD IDord-55bb1e8f570f42b7b39a2ad831b1a37b
출처 메모uspto-grants-1992_10