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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanesulfonamide, N-(aminosulfonyl)-N-methyl- | HCID 11084607 | — |
| 반응물 | Phenyl (4-methoxy-6-methylpyrimidin-2-yl)carbamate | HCID 13577349 | — |
| 용매 | Chlorobenzene | HCID 7964 | — |
| 생성물 | 1-[(N-Methylsulfonyl-N-methylamino)sulfonyl]-3-(4-methoxy-6-methyl-2-pyrimidyl)urea | HCID 13371783 | 96.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05155222 |
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| 출처 데이터셋 | uspto-grants-1992_10 |
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| ORD ID | ord-55bb1e8f570f42b7b39a2ad831b1a37b |
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| 출처 메모 | uspto-grants-1992_10 |
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