HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 6-Methoxy-3-trifluoromethanesulfonyloxy-quinoline-4-carboxylic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | Methyl 3-hydroxy-6-methoxyquinoline-4-carboxylate | HCID 46912076 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Methoxy-3-trifluoromethanesulfonyloxy-quinoline-4-carboxylic acid methyl ester | HCID 86671528 | 76% |
Reaction Steps
Trifluoromethanesulfonic anhydride (3.35 mL, 19.94 mmol, 1.5 eq) is added at room temperature to a stirred solution of 3-hydroxy-6-methoxy-quinoline-4-carboxylic acid methyl ester (3.1 g, 13.29 mmol, 1.0 eq) in dichloromethane (30 mL), followed by triethylamine (5.6 mL, 39.88 mmol, 3.0 eq). After 1 hour stirring at room temperature, solvent is removed and the residue is purified by column chromatography (silica gel, eluent: petroleum ether:ethyl acetate, 5:1, v/v) to afford 6-methoxy-3-trifluoromethanesulfonyloxy-quinoline-4-carboxylic acid methyl ester as a yellow solid (3.69 g, 76% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08927541B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-43216227d73a4d79ba549cc5b4bfb3d8 |
| Source note | uspto-grants-2015_01 |