HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466747Generated: October 25, 2026
4-Methoxy-6-methylpyrimidin-2-amine → 1-[(N-Methylsulfonyl-N-methylamino)sulfonyl]-3-(4-methoxy-6-methyl-2-pyrimidyl)urea
https://huagongshe.com/reaction/466747
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxy-6-methylpyrimidin-2-amine | HCID 587236 | — |
| Reactant | ethyl (N-methylsulfonyl-N-methylamino)sulfonylcarbamate | HCID 53920146 | — |
| 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
52.0 g of ethyl (N-methylsulfonyl-N-methylamino)sulfonylcarbamate are dissolved in 500 ml of chlorobenzene, 27.8 g of 2-amino-4-methoxy-6-methylpyrimidine are added at room temperature, and the mixture is heated at 50° C. for 5 hours. After cooling to 0° C., the precipitate is filtered off. After washing with 100 ml of chlorobenzene, 68.8 g of the desired product of a purity of 98.9% 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 |
|---|
| Patent number | US05157121 |
|---|
| Source dataset | uspto-grants-1992_10 |
|---|
| ORD ID | ord-75afe0bdbbf8443d95583a02e8f33005 |
|---|
| Source note | uspto-grants-1992_10 |
|---|