HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-aminoquinoline-3-carboxylate → Ethyl 3,4-dihydro-4-oxopyrimido(4,5-b)quinoline-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-aminoquinoline-3-carboxylate | HCID 283477 | — |
| Reactant | 1-Carbethoxyformimidate | HCID 22752822 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3,4-dihydro-4-oxopyrimido(4,5-b)quinoline-2-carboxylate | HCID 135765023 | — |
Reaction Steps
The same compound is obtained by: (a) refluxing equimolar amounts of 1-carbethoxyformimidate and ethyl 2-aminoquinoline-3-carboxylate in ethanol for three hours. The reaction mixture is concentrated, the product collected by filtration and recrystallized from hot chloroform; or (b) refluxing equimolar amounts of 1-carbethoxyformamidine and 2-aminoquinoline-3-carboxamide in ethanol for 3-4 hours in the presence of an equimolar amount of sodium ethoxide. The reaction mixture is worked up as described in (a) above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03974161 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-f606fbcb748f4804817a9a76bb3fe748 |
| Source note | uspto-grants-1976_08 |