HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → Methyl 7-(benzyloxy)-4-chloro-6-quinolinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Methyl 7-(benzyloxy)-4-oxo-1,4-dihydro-6-quinolinecarboxylate | HCID 22936245 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 7-(benzyloxy)-4-chloro-6-quinolinecarboxylate | HCID 22936661 | — |
Reaction Steps
After adding thionyl chloride (70 ml) and a catalytic amount of dimethylformamide to methyl 7-(benzyloxy)-4-oxo-1,4-dihydro-6-quinolinecarboxylate (7.19 g, 23.2 mmol), the mixture was heated to reflux for 3 hours while stirring. The reaction solution was concentrated under reduced pressure, a 2N sodium hydroxide solution was gradually added for neutralization, extraction was performed with ethyl acetate, and the organic layer was washed with water and saturated brine and dried over anhydrous sodium sulfate. The solvent was distilled off, diethyl ether was added for crystallization, and the crystals were filtered out and blow-dried to obtain the title compound (4.067 g, 12.4 mmol) as light brown crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07253286B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-9c0f573d170143539cb201886186ceb3 |
| Source note | uspto-grants-2007_08 |