HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466255Generated: October 26, 2026
Methanesulfonamide, N-(aminosulfonyl)-N-methyl- → 1-[(N-Methylsulfonyl-N-methylamino)sulfonyl]-3-(4-methoxy-6-methyl-2-pyrimidyl)urea
https://huagongshe.com/reaction/466255
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonamide, N-(aminosulfonyl)-N-methyl- | HCID 11084607 | — |
| Reactant | Phenyl (4-methoxy-6-methylpyrimidin-2-yl)carbamate | HCID 13577349 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 1-[(N-Methylsulfonyl-N-methylamino)sulfonyl]-3-(4-methoxy-6-methyl-2-pyrimidyl)urea | HCID 13371783 | 96.4% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05155222 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-55bb1e8f570f42b7b39a2ad831b1a37b |
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| Source note | uspto-grants-1992_10 |
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