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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711671Generated: October 25, 2026

4-Methoxybenzylamine → 4-Amino-2-oxo-1,2-dihydroquinoline-3-carbonitrile

https://huagongshe.com/reaction/711671

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzylamineHCID 75452—
Reactant4-Chloro-1,2-dihydro-2-oxoquinoline-3-carbonitrileHCID 2777510—
SolventDimethylformamideHCID 6228—
Product4-Amino-2-oxo-1,2-dihydroquinoline-3-carbonitrileHCID 520031225.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

4-chloro-2-oxo-1,2-dihydroquinoline-3-carbonitrile (example 72) (0.66 g, 3.23 mmol) was suspended in DMF (7 mL), and 4-methoxybenzylamine (0.94 mL, 7.26 mmol) was added. The reaction was heated at 100° C. for 1 hour and the DMF was removed under vacuum. The residue was dissolved in TFA (6 mL) and stirred at room temperature for 30 minutes and dichloromethane (10 mL) was added. The solid product that formed was collected, suspended in water and the solution stirred overnight. The solid was collected by filtration to give 4-amino-2-oxo-1,2-dihydroquinoline-3-carbonitrile (0.150 g, 25%) as a white solid. M.p.: >250° C. 1H NMR (400 MHz, DMSO-d6) δ 7.19 (m, 2H), 7.57 (m, 1H), 7.88 (bs, 2H), 8.12 (d, J=7.6 Hz, 1H), 11.23 (s, 1H). MS 186 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181276B2
Source datasetuspto-grants-2015_11
ORD IDord-35534af4bc214111bacea8dea69db3ac
Source noteuspto-grants-2015_11