HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl-1,3,5-triazin-2-amine → N-[(4,6-dimethyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-chlorobenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl-1,3,5-triazin-2-amine | HCID 15820 | — |
| Reactant | Benzenesulfonyl isocyanate, 2-chloro- | HCID 174071 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-[(4,6-dimethyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-chlorobenzenesulfonamide | HCID 13883435 | — |
Reaction Steps
To 12.3 g of 2-amino-4,6-dimethyl-1,3,5-triazine in 200 ml of acetonitrile was added with stirring 21.7 g of 2-chlorobenzenesulfonyl isocyanate. All of the solid dissolved after the reagents were added and the mixture was then evaporated to dryness. The solid residue was triturated with ethyl ether and isolated by filtration to give impure N-[(4,6-dimethyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-chlorobenzenesulfonamide melting at 115°-118° C. The nuclear magnetic resonance absorption spectrum of this product, in trifluoroacetic acid, showed singlet peaks at 2.69 and 2.9 parts per million.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04127405 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-903d03d780f1417ea07cca14fe89c1a4 |
| Source note | uspto-grants-1978_11 |