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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507046Generated: October 31, 2026

Ethyl (quinolin-8-yloxy)acetate → N-(2-hydroxy-3-(isoindolin-2-yl)propyl)-2-(quinolin-8-yloxy)acetamide

https://huagongshe.com/reaction/1507046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl (quinolin-8-yloxy)acetateHCID 4379860—
Reactant1-Amino-3-(isoindolin-2-yl)propan-2-olHCID 62206063—
SolventEthanolHCID 702—
ProductN-(2-hydroxy-3-(isoindolin-2-yl)propyl)-2-(quinolin-8-yloxy)acetamideHCID 7690241518%

Reaction Conditions

Temperature120 °C

Reaction Steps

1-amino-3-(isoindolin-2-yl)propan-2-ol (50 mg, 0.26 mmol) and ethyl 2-(quinolin-8-yloxy)acetate (60 mg, 0.26 mmol) were dissolved in EtOH (1 mL) and heated under microwave conditions at 120° C. for 0.5 h. The reaction mixture was concentrated and purified by preparative HPLC purification. (17.2 mg, yield 18%) MS (ESI+) e/z: 378.1 [M+1]+. 1H NMR (MeOD, 400 MHz), δ ppm: 8.95-8.87 (m, 1H), 8.45-8.36 (m, 1H), 7.67-7.56 (m, 3H), 7.35-7.25 (m, 1H), 7.24-7.12 (m, 4H), 4.83-4.76 (m, 2H), 4.09-4.03 (m, 1H), 4.02-3.95 (m, 4H), 3.60-3.54 (m, 1H), 3.46-3.40 (m, 1H), 2.92-2.86 (m, 1H), 2.84-2.78 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221794B2
Source datasetuspto-grants-2015_12
ORD IDord-b3876141ef124ff1b8746e1a4a0adc52
Source noteuspto-grants-2015_12