HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-4-methoxy-6-methyl-1,3,5-triazine → Metsulfuron-methyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-4-methoxy-6-methyl-1,3,5-triazine | HCID 15466 | — |
| Reactant | Benzoic acid, 2-(isocyanatosulfonyl)-, methyl ester | HCID 156281 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Metsulfuron-methyl | HCID 52999 | — |
Reaction Steps
To an anhydrous suspension of 1.4 g of 2-amino-4-methoxy-6-methyl-1,3,5-triazine in 25 ml of methylene chloride was added with stirring at ambient temperature and pressure 2.4 g of 2-methoxycarbonylbenzenesulfonylisocyanate. The mixture was thereafter stirred for 16 hours and filtered. The filtrate was evaporated to dryness, the residue was triturated with butyl chloride and the product removed by filtration. The product thus obtained melted at 165°, and had absorption peaks in the infrared at 1550, 1600, 1680 and 1700 cm-1 and in the NMR spectrum at 2.5, 3.65, 4.0 with an aromatic multiplet at 7.2-8 ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04536576 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-ecc0819040fb402aa34064dd0df307fa |
| Source note | uspto-grants-1985_08 |