HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-4-methoxy-6-methyl-1,3,5-triazine → HCID 13729507, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-4-methoxy-6-methyl-1,3,5-triazine | HCID 15466 | — |
| Reactant | HCID 86741548 | HCID 86741548 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | HCID 13729507 | HCID 13729507 | — |
Reaction Steps
A solution of 1.48 g of N-(2-difluoromethoxy-phenylsulfonyl)-ethylcarbamate and 0.62 g of 2-amino-4-methoxy6-methyl-1,3,5-triazine in 20 ml of chlorobenzene is refluxed. After concentration of the yellow solution by evaporation, and chromatographical purification of the residue, there is obtained a colourless oil which crystallises from an acetone/diethyl ether mixture by the addition of hexane. The yield is 0.45 g (23.1% of theory) of N-(2-difluoromethoxyphenylysulfonyl)-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-urea, m.p. 140°-141° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04668800 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-c946fd86d10443698ed89472a2163600 |
| Source note | uspto-grants-1987_05 |