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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076279Generated: November 1, 2026

(R)-(-)-1-Aminoindan → [5-(4-Fluoro-benzyloxy)-quinolin-2-yl]-(R)-indan-1-yl-amine

https://huagongshe.com/reaction/2076279

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-(-)-1-AminoindanHCID 2733933—
Reactant2-Chloro-5-(4-fluoro-benzyloxy)-quinolineHCID 86619496—
Product[5-(4-Fluoro-benzyloxy)-quinolin-2-yl]-(R)-indan-1-yl-amineHCID 67095974—

Reaction Steps

2-Chloro-5-(4-fluoro-benzyloxy)-quinoline (100 mg, 0.347 mmol) and (R)-1-aminoindane (138 mg, 1.04 mmol) were stirred in a sealed tube at 150° C. overnight. The reaction mixture was purified by flash chromatography on silica gel (heptane/ethyl acetate 75:25). The title compound was obtained as a light brown oil (68 mg, 51%), MS: m/e=385 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923561B2
Source datasetuspto-grants-2011_04
ORD IDord-4f11c968eed24962ab403eacf1b0d1c4
Source noteuspto-grants-2011_04