HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methane → HCID 178494213, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Metsulfuron-methyl | HCID 52999 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 178418311 | HCID 178418311 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178494213 | HCID 178494213 | — |
Reaction Steps
To a slurry of 4.0 g of N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-methoxycarbonylbenzenesulfonamide in 100 ml of methylene chloride was added by syringe 10 ml of a 2M solution of trimethylaluminum in toluene (1.44 g of Al(CH3)3). Evolution of methane gas was seen. 3-Amino-1,2,4-triazole (1.7 g) was then added and the mixture was heated at reflux for 18 hours. The reaction mixture was then treated with aqueous hydrochloric acid and the precipitated product was purified by trituration in methylene chloride, 0.63 g, m.p. 176°-179° C. NMR in TFA 2.9 ppm s, CH3 on triazine, 4.4 ppm s, OCH3 on triazine, 7.8-8.0 ppm and 8.2-8.5 ppm M, aromatic.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04555261 |
| Source dataset | uspto-grants-1985_11 |
| ORD ID | ord-e98b86d30c0c458c80e6e4c941142d1d |
| Source note | uspto-grants-1985_11 |