HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 20262853, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Oxalic Acid | HCID 971 | — |
| Reactant | HCID 15426392 | HCID 15426392 | — |
| Reactant | HCID 20262851 | HCID 20262851 | — |
| Product | HCID 20262853 | HCID 20262853 | — |
Reaction Steps
4-(2-Chlorophenyl)-3-(ethoxycarbonyl)-3-(methoxycarbonyl)-6-methyl-2-[2-(piperazin-1-yl)ethoxymethyl]-1,4-dihydropyridine (0.7 g) was dissolved in 10 ml of ethanol and converted to the oxalate salt by addition of a solution of 0.15 g of oxalic acid in 5 ml of ethanol. To this suspension was added 0.12 g of 2-ethoxypyrroline and the mixture was refluxed for 18 hours. The reaction mixture was then filtered through "Solka-floc" (Trade Mark) and evaporated to dryness. The resultant solid was basified with aqueous sodium carbonate solution and extracted with methylene chloride to give a white solid. After two crystallizations from diisopropylether, there was obtained 0.1 g of the title compound, m.p. 104°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04547502 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-1db1243a7fb042ec9ab81c5a27b855a0 |
| Source note | uspto-grants-1985_10 |