HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 15586997, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | O-mesitylenesulfonylhydroxylamine | HCID 11009332 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178503529 | HCID 178503529 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15586997 | HCID 15586997 | 81.3% |
Reaction Steps
To a solution of 3-methylthio-6-(p-fluorophenyl)-5-oxo-2,5-dihydro-1,2,4-triazine (2.5 g) in anhydrous dimethylformamide (50 ml), sodium hydride (50% dispersion, 0.5 g) was gradually added and stirred until the generation of hydrogen gas was not detected. o-Mesitylenesulfonylhydroxylamine (2.1 g) was added to the mixture, followed by stirring at room temperature for 6 hours. After completion of the reaction, the resultant mixture was poured into ice-water. The precipitated crystals were collected by filtration. Recrystallization of the obtained crystals from methanol gave 2.0 g of 2-amino-3-methylthio-6-(p-fluorophenyl)-5-oxo-2,5-dihydro-1,2,4-triazine in 74% yield. M.P., 192° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04451283 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-f84ee8f086754f6c87c4c9fad2b196a8 |
| Source note | uspto-grants-1984_05 |