Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 20232098 | HCID 20232098 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 23326429 | HCID 23326429 | — |
Reaction Steps
A solution of 3-carboxymethylthio-5-methyl-6-(1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-1,2,4-triazine (7.25 g) in a mixture of 10% aqueous solution of potassium hydroxide (47 ml) and methanol (47 ml) was heated at 60° for 4 hours with stirring. To the mixture were added potassium iodide (0.5 g), benzyl chloride (5.33 g), and methanol (150 ml), refluxed for 8 hours with stirring, and evaporated in vacuo. To the residue was added water and extracted with ethyl acetate. The extract was dried over magnesium sulfate and evaporated in vacuo. The oily residue was purified by column chromatography on silica gel (300 g) with ethyl acetate as an eluent to give 6-(1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-2-benzyl-5-methyl-1,2,4-triazin-3(2H)-one (4.47 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04581356 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-eeea2965d88f43c58be4f787d08a148c |
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| Source note | uspto-grants-1986_04 |
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