HuagongsheHuagongshe Chemistry Print Report · For research reference only
Malonic Acid → Ethyl 3-(6-methyl-3-pyridyl)propionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Malonic Acid | HCID 867 | — |
| Reactant | 6-Methyl-3-pyridinecarboxaldehyde | HCID 10192566 | — |
| Reactant | 3-(6-Methyl-3-pyridyl)acrylic acid | HCID 54140853 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Ethyl 3-(6-methyl-3-pyridyl)propionate | HCID 3018102 | — |
Reaction Steps
3-(6-Methyl-3-pyridyl)propenoic acid, m.p. 213.5-215.5°, was prepared by reacting 6-methylpyridine-3-carboxaldehyde with malonic acid in pyridine with piperidine catalyst, and was converted into the corresponding ethyl ester m.p. 36°-37° which was reduced with hydrogen and palladium-on-charcoal catalyst to give ethyl 3-(6-methyl-3-pyridyl)-propionate (oil). This ester was reacted with sodium and ethyl formate and the product treated with thiourea to give 5-(6-methyl-3-pyridylmethyl)-2-thiouracil m.p. 240°-241° which was alkylated with methyl iodide in the presence of sodium hydroxide at 70° to give 5-(6-methyl-3-pyridylmethyl)-2-methylthio-4-pyrimidone, m.p. 197°-198.5°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04558128 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-e18a9497d06b476c944cdc5afc2b2e64 |
| Source note | uspto-grants-1985_12 |