Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 3-Quinolineacrylate | HCID 78434631 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | Ethyl 3-quinolinepropionate | HCID 14338577 | — |
Reaction Steps
3-quinolineacrylate (51.68 g) was dissolved in ethanol (170 ml) and hydrogenated at 37° and a pressure of 50 psi using 10% Palladium on charcoal to give ethyl 3-quinolinepropionate. p (iii) Ethyl 3-quinolinepropionate (47.99 g) and ethyl formate (16.3 g) were added over a period of 3 hours to a stirred mixture of sodium wire (4.8 g) and dry ether (150 ml) cooled by an ice-bath. The mixture was stirred for 20 hours at room temperature, evaporated to dryness and the residue was treated with thiourea (15.9 g) and ethanol (130 ml) and refluxed for 7 hours. The mixture was evaporated to dryness and the residue was dissolved in water and acetic acid added to pH 4. The mixture was filtered to give 5-(3-quinolinemethyl)-2-thiouracil, m.p. 281°-6° (decomp.) (ex. acetic acid-water).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04216318 |
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| Source dataset | uspto-grants-1980_08 |
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| ORD ID | ord-d83076b2d3994fa9a7f6ee95cdf3bc9f |
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| Source note | uspto-grants-1980_08 |
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