HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(1-methyl-1H-pyrazol-4-yl)benzenesulfonamide → N-[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-(1-methyl-1H-pyrazol-4-yl)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(1-methyl-1H-pyrazol-4-yl)benzenesulfonamide | HCID 13489814 | — |
| Reactant | Methyl (4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamate | HCID 14404501 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-(1-methyl-1H-pyrazol-4-yl)benzenesulfonamide | HCID 13489865 | 17.6% |
Reaction Steps
By the procedure of Example 14, 2 g of 2-(1-methyl-1H-pyrazol-4-yl)benzenesulfonamide, prepared in Example 19, was reacted in 100 ml of methylene chloride with 0.7 g of trimethylaluminum (5 ml of 2M toluene solution) followed by 1.7 g of methyl (4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamate. After work up and evaporation of the methylene chloride solvent, the residue was triturated with ethyl acetate to yield 0.6 g of the title compound; m.p. 221°-224° C. The IR spectrum showed a carbonyl absorption at 1700 cm-1 indicative for a sulfonylurea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04511392 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-70198f55f61f447c819e7aa38bdd886a |
| Source note | uspto-grants-1985_04 |