HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → Ethyl 8-aminoquinoline-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | Ethyl 4-chloro-8-nitroquinoline-3-carboxylate | HCID 11196760 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 8-aminoquinoline-3-carboxylate | HCID 21250128 | 58% |
Reaction Steps
Ammonium formate was added to a vigorously stirred mixture of 4-chloro-3-ethoxycarbonyl-8-nitro-quinoline (5.6 g), ethanol (1000 ml) and 10% palladium on carbon catalyst (2 g). The mixture was stirred at ambient temperature for 1 hour, filtered through a pad of celite and the pad washed with dichloromethane. The combined filtrate and washings were evaporated to dryness. The residue so obtained was purified by flash chromatography on silica using chloroform as eluant to give 3-ethoxycarbonyl-8-amino-quinoline in 58% yield, mp 94-96° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05916898 |
| Source dataset | uspto-grants-1999_06 |
| ORD ID | ord-7a1ce72d16c0489c89aba36e3aff8d0b |
| Source note | uspto-grants-1999_06 |