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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471529Generated: October 30, 2026

HCID 67097724, compound → Methyl 4-amino-2-oxo-1,2-dihydroquinoline-3-carboxylate

https://huagongshe.com/reaction/471529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67097724HCID 67097724—
SolventTrifluoroacetic acidHCID 6422—
ProductMethyl 4-amino-2-oxo-1,2-dihydroquinoline-3-carboxylateHCID 65817342.3%

Reaction Steps

Methyl 4-(4-methoxybenzylamino)-2-oxo-1,2-dihydroquinoline-3-carboxylate (Example 68a) (0.841 g, 2.49 mmol) was dissolved in TFA (5 mL) and stirred at room temperature for 30 minutes. The TFA was removed under reduced pressure, and the residue was dissolved in dichloromethane, then precipitated out by adding excess diethyl ether. The resultant solid was collected by filtration, suspended in dichloromethane, and washed with concentrated sodium bicarbonate. The solid was collected to give methyl 4-amino-2-oxo-1,2-dihydroquinoline-3-carboxylate (0.230 g, 42%) as a white solid. M.p.: 236° C. 1H NMR (400 MHz, DMSO-d6) δ 3.73 (s, 3H), 7.12 (t, J=8.0 Hz, 1H), 7.17 (d, J=8.0 Hz, 1H), 7.52 (t, J=8.0 Hz, 1H), 8.08 (d, J=8.0 Hz, 1H), 8.38 (bs, 2H), 10.88 (bs, 1H). MS 219 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633186B2
Source datasetuspto-grants-2014_01
ORD IDord-690e0c90c22848ce83d027798f436bd9
Source noteuspto-grants-2014_01