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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44396Generated: October 28, 2026

HCID 57456934, compound → 4-amino-2-oxo-1,2-dihydroquinoline-3-carboxylic acid

https://huagongshe.com/reaction/44396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57456934HCID 57456934—
CatalystPalladiumHCID 23938—
SolventDimethylformamideHCID 6228—
Product4-amino-2-oxo-1,2-dihydroquinoline-3-carboxylic acidHCID 59482112%

Reaction Steps

Benzyl 4-amino-2-oxo-1,2-dihydroquinoline-3-carboxylate (Example 66a) (0.6 g, 2.04 mmol) was dissolved in DMF (8 mL) and heated at 70° C. under a hydrogen balloon in the presence of 10% Pd/C (0.15 g) for 1 hour. The Pd/C was filtered out and washed with dichloromethane and the solvents were removed under vacuum. The residue was dissolved/suspended in NaOH (2M, 40 mL), stirred at room temperature for 30 minutes and the solution washed with dischloromethane. The aqueous layer was cooled to 0° C. and acidified to pH 1 with 2M HCl. The resultant precipitate was collected and washed with dichloromethane to give 4-amino-2-oxo-1,2-dihydroquinoline-3-carboxylic acid (0.050 g, 12%) as a light yellow solid. M.p.: >250° C. 1H NMR (400 MHz, DMSO-d6) δ7.32 (m, 1H), 7.39 (d, J=7.6 Hz, 1H), 7.69 (m, 1H), 8.27 (d, J=8.4 Hz, 1H), 8.86 (s, 1H), 9.87 (s, 1H), 11.95 (s, 1H). MS 205 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541421B2
Source datasetuspto-grants-2013_09
ORD IDord-6a0827da57834f37b5ef678db07a7b5b
Source noteuspto-grants-2013_09