HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 13469424, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 6-(4-aminophenyl)-5-methyl-4,5-dihydro-1,2,4-triazin-3(2H)-one | HCID 13386033 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 13469424 | HCID 13469424 | 64.4% |
Reaction Steps
Chloroacetyl chloride (1.25 g) was added dropwise to a solution of 6-(4-aminophenyl)-5-methyl-4,5-dihydro-1,2,4-triazin-3(2H)-one (2.04 g) and triethylamine (1.01 g) in DMF (10 ml) and then stirred for 30 minutes. To the stirred solution were added potassium iodide (0.53 g) and morpholine (4.53 g). The reaction mixture was stirred for 30 minutes and then evaporated in vacuo. To the residue was added water and the resultant solid was collected by filtration, washed with water and recrystallized from aqueous ethanol to give 6-[4-(2-morpholinoacetamido)phenyl]-5-methyl-4,5-dihydro-1,2,4-triazin-3(2H)-one (2.13 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04616015 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-5c2864e07ca8489b9d03fc779e6de818 |
| Source note | uspto-grants-1986_10 |