HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36388Generated: October 26, 2026
2-Amino-4,6-dimethoxypyrimidine → Amidosulfuron
https://huagongshe.com/reaction/36388
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Amino-4,6-dimethoxypyrimidine | HCID 118946 | — |
| Reactant | 1-[(N-methylsulfonyl-N-methylamino)-sulfonyl]-3-(N-methylsulfonyl-N-methylamino)urea | HCID 23373886 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | Amidosulfuron | HCID 91777 | 103.2% |
Reaction Steps
32.3 g of 1-[(N-methylsulfonyl-N-methylamino)-sulfonyl]-3-(N-methylsulfonyl-N-methylamino)urea are slurried in 500 ml of chlorobenzene, 15.5 g of 2-amino-4,6-di-methoxypyrimidine are added at 80° C. with stirring, and the mixture is heated for 3 hours at 80° C. After cooling to 20° C., the precipitate is filtered off and washed with 100 ml of chlorobenzene. 36.4 g of the desired product are obtained with a purity of 98.1%, corresponding to a yield of 96.8% of theory. The melting point for the product is 183°-185° C. 5.1 g of N-methylmethanesulfonamide are recovered from the filtrate by distillation, corresponding to a yield of 92.7% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05414084 |
|---|
| Source dataset | uspto-grants-1995_05 |
|---|
| ORD ID | ord-06b25bb0346b4fd7a734e7384a16ca50 |
|---|
| Source note | uspto-grants-1995_05 |
|---|