Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Pyrido[3,2-g]quinoline-2,8-dicarboxylic acid | HCID 13143645 | — |
| Solvent | Diethylene Glycol Monomethyl Ether | HCID 8134 | — |
| Product | Pyrido[3,2-g]quinoline | HCID 2750235 | — |
Reaction Steps
Diethylene glycol monomethyl ether (20 cc) was added to pyrido[3,2-g] quinoline-2,8-dicarboxylic acid (2.01 g, 7.5 mmol) from the above process and cuprous oxide (I) (50 mg, 0.35 mmol), and heated for 5.5 hours at 165° C. Carbon dioxide evolved during the reaction. After the addition of conc. aquous ammonia (25 cc), extracted with dichloromethane (3×100 ml) and dried on potassium carbonate and evaporated dichloromethane to yield pyrido[3,2-g]quinoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05091535 |
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| Source dataset | uspto-grants-1992_02 |
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| ORD ID | ord-958bb5393eca46f4a05a7018a97f9e3e |
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| Source note | uspto-grants-1992_02 |
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