HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfate → 1-methyl-6-(3-pyridyl)-2-(1H)-quinolone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-(3-pyridyl)-2-(1H)-quinolone | HCID 9991095 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-methyl-6-(3-pyridyl)-2-(1H)-quinolone | HCID 13728856 | — |
Reaction Steps
A stirred solution of 6-(3-pyridyl)-2-[1H]-quinolone (0.05 g) in DMF (0.5 cm3) was treated at room temperature with sodium hydride (0.012 g of a 50% dispersion in oil) for 1 hour. A solution of dimethyl sulphate (0.016 g) in DMF (0.2 cm3) was added and the mixture was stirred for 1.5 hours. The mixture was concentrated in vacuo, water (5 cm3) was added and the mixture was extracted with ethyl acetate (3×10 cm3). The combined organic extracts were dried (MgSO4), concentrated in vacuo and the residue chromatographed on silica (Merck "MK 60.9385") eluting with chloroform to yield a solid which was triturated with ether to afford 1-methyl-6-(3-pyridyl)-2-(1H)-quinolone 0.25H2O, m.p. 116°-118°, (0.02 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04710507 |
| Source dataset | uspto-grants-1987_12 |
| ORD ID | ord-d4eecf49b6734a2485ef314a7c5a0ccb |
| Source note | uspto-grants-1987_12 |