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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170123Generated: November 1, 2026

2-Methoxybenzylamine → 5-(4-Fluorobenzyloxy)-quinolin-2-yl-(2-methoxy-benzyl)-amine

https://huagongshe.com/reaction/1170123

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxybenzylamineHCID 81292—
Reactant2-Chloro-5-(4-fluoro-benzyloxy)-quinolineHCID 86619496—
Product5-(4-Fluorobenzyloxy)-quinolin-2-yl-(2-methoxy-benzyl)-amineHCID 67334651—

Reaction Steps

2-Chloro-5-(4-fluoro-benzyloxy)-quinoline (100 mg, 0.35 mmol) and 2-methoxybenzylamine (144 mg, 1.05 mmol) were stirred in a sealed tube at 150° C. for 16 hours. The reaction mixture was purified by flash chromatography on silica gel (heptane/ethyl acetate 100:0->80:20 gradient). 5-(4-Fluorobenzyloxy)-quinolin-2-yl-(2-methoxy-benzyl)-amine was obtained as a yellow oil (57 mg, 42%), MS: m/e=389.3 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825253B2
Source datasetuspto-grants-2010_11
ORD IDord-a050bf34850b4d77aea020c8fa6f4d4b
Source noteuspto-grants-2010_11