HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl formate → HCID 12783848, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Ethyl 3-(6-methyl-3-pyridyl)propionate | HCID 3018102 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Product | HCID 12783848 | HCID 12783848 | — |
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-6190d7b53bcf47a882d9b9e1ee4682c8 |
| Source note | uspto-grants-1985_12 |