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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748375Generated: October 30, 2026

HCID 90417413, compound → HCID 136629534, compound

https://huagongshe.com/reaction/1748375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 90417413HCID 90417413—
ReactantHCID 90417428HCID 90417428—
ReactantHCID 90417558HCID 90417558—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 136629534HCID 13662953435%

Reaction Steps

Ethyl 2-(7-methoxyquinolin-3-yl)acetate. To a solution of a crude mixture of ethyl 2-(2-chloro-7-methoxyquinolin-3-yl)acetate and ethyl 2-(2-chloro-5-methoxyquinolin-3-yl)acetate in EtOAc (200 mL) and EtOH (200 mL) was added 10% Pd/C (50 mg, 0.47 mmol). The reaction mixture was placed under an atmosphere of hydrogen and stirred at ambient temperature for 3 days. The crude reaction mixture was filtered through silica and concentrated to afford a brown oil. Purification by FCC (SiO2, 0-5%, MeOH/DCM) yielded the title compound as a light brown solid (6.0 g, 35% over 2 steps). 1H NMR (400 MHz, CDCl3) δ 8.76 (d, J=2.0 Hz, 1H), 8.00 (d, J=2.3 Hz, 1H), 7.67 (d, J=8.6 Hz, 1H), 7.41 (d, J=2.3 Hz, 1H), 7.20 (dd, J=9.0, 2.3 Hz, 1H), 4.18 (q, J=7.2 Hz, 2H), 3.95 (s, 3H), 3.76 (s, 2H), 1.26 (t, J=6.8 Hz, 3H). [M+H]=246.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150572B2
Source datasetuspto-grants-2015_10
ORD IDord-898dfd2ed44848e69dc8b540c2e8cabc
Source noteuspto-grants-2015_10