HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-4,6-dimethoxy-1,3,5-triazine → N-[(4,6-dimethoxy-1,3,5-triazin-2-yl)aminocarbonyl]-2-chlorobenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-4,6-dimethoxy-1,3,5-triazine | HCID 27840 | — |
| Reactant | Benzenesulfonyl isocyanate, 2-chloro- | HCID 174071 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[(4,6-dimethoxy-1,3,5-triazin-2-yl)aminocarbonyl]-2-chlorobenzenesulfonamide | HCID 14835175 | — |
Reaction Steps
To 15.6 g of 2-amino-4,6-dimethoxy-1,3,5-triazine in 300 ml of dry methylene chloride containing 0.1 g 1,4-diazabicyclo[2,2,2]octane was added 21 g 2-chlorobenzenesulfonyl isocyanate with stirring. The mixture was stirred for 16 hours and the resultant solid was removed by filtration. After washing the solid with 1-chlorobutane, the resulting product, N-[(4,6-dimethoxy-1,3,5-triazin-2-yl)-aminocarbonyl]-2-chlorobenzenesulfonamide melted at 188°-189° C. Infrared absorption analysis showed absorption peaks at 1740 cm-1, 1630 cm-1 and 1595 cm-1 which are typical for this type of compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04127405 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-3f5511fb26d5403e9c89d6032cc99f9b |
| Source note | uspto-grants-1978_11 |