HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl (ethoxymethylene)malonate → HCID 21829132, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | p-Phenetidine, 3-methoxy- | HCID 209360 | — |
| Product | HCID 21829132 | HCID 21829132 | 55.2% |
Reaction Steps
4-Ethoxy-3-methoxyaniline (2.6 g) and diethyl ethoxymethylenemalonate (3.4 g) were reacted in the same manner as in Experimental Example 1 to obtain 6-ethoxy-3-ethoxycarbonyl-7-methoxy-4(1H)-quinolone (2.5 g). The compound (2.3 g) was ethylated with potassium carbonate (3.3 g) and ethyl iodide (6.1 g) in the same manner as in Experimental Example 9 to obtain 6-ethoxy-3-ethoxycarbonyl-1-ethyl-7-methoxy-4(1H)-quinolone (1.8 g). This compound (1.4 g) was hydrolyzed in the same manner as in Experimental Example 9 to obtain a carboxylic acid (1.2 g), which was then decarboxylated in the same manner as in Experimental Example 9 to obtain 6-ethoxy-1-ethyl-7-methoxy-4(1H)-quinolone (compound 49, 210 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05081121 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-4c797cd740794b8eaae4557ec0696953 |
| Source note | uspto-grants-1992_01 |