HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoic acid, 2-(isocyanatosulfonyl)-, methyl ester → 6-[3-(2-Methoxycarbonylphenylsulfonyl)-ureido]-4-methyl-3-methylthio-1,2,4-triazin-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoic acid, 2-(isocyanatosulfonyl)-, methyl ester | HCID 156281 | — |
| Reactant | 6-Amino-4-methyl-3-(methylsulfanyl)-1,2,4-triazin-5(4H)-one | HCID 11542851 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-[3-(2-Methoxycarbonylphenylsulfonyl)-ureido]-4-methyl-3-methylthio-1,2,4-triazin-5-one | HCID 19856563 | 73.1% |
Reaction Steps
3.42 g of 6-amino-4-methyl-3-methylthio-1,2,4-triazin-5-one are suspended in 100 ml of absolute dioxane, and 4.99 g of 2-methoxycarbonylphenylsulfonyl isocyanate are added at room temperature. The reaction proceeds slightly exothermically. After a reaction time of one hour at room temperature, the reaction has ended. The precipitate which has separated out is filtered off and washed with a small amount of dioxane. After drying, 6.0 g of 6-[3-(2-methoxycarbonylphenylsulfonyl)-ureido]-4-methyl-3-methylthio-1,2,4-triazin-5-one with a melting point of 186°-187° C. are thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04795486 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-5d58e8e3385d436c9b79529576b7c8d9 |
| Source note | uspto-grants-1989_01 |