HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dioxane → {2-ethyl-8-fluoro-3-[4-(morpholine-4-sulfonyl)benzyl]-4-oxo-1,4-dihydroquinolin-5-yloxy}acetic Acid Methyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | (3-Amino-4-fluorophenoxy)acetic acid methyl ester | HCID 66717607 | — |
| Reactant | 2-[4-(morpholine-4-sulfonyl)benzyl]-3-oxopentanoic Acid Methyl Ester | HCID 68784251 | — |
| Solvent | Water | HCID 962 | — |
| Product | {2-ethyl-8-fluoro-3-[4-(morpholine-4-sulfonyl)benzyl]-4-oxo-1,4-dihydroquinolin-5-yloxy}acetic Acid Methyl Ester | HCID 68783164 | — |
Reaction Conditions
| Temperature | 130 °C |
|---|
Reaction Steps
A mixture of (3-amino-4-fluorophenoxy)acetic acid methyl ester (0.22 g), 2-[4-(morpholine-4-sulfonyl)benzyl]-3-oxopentanoic acid methyl ester (0.41 g), polyphosphoric acid (1 g) and dioxane (20 mL) was heated at 130° C. for 18 hours. The mixture was cooled to room temperature, diluted with water and extracted with ethyl acetate. The combined extracts were dried over magnesium sulfate and the solvent removed under reduced pressure. The residue was purified by column chromatography on silica gel, eluting with a mixture of ethyl acetate, dichloromethane and methanol (1:4:0 to 1:1:0 to 0:9:1 by volume) to afford title compound, 0.14 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858640B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-faa5e49a3e7a4a149e18c721f7263a20 |
| Source note | uspto-grants-2010_12 |