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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931474Generated: November 4, 2026

(R)-(-)-1-Aminoindan → HCID 44217313, compound

https://huagongshe.com/reaction/1931474

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-(-)-1-AminoindanHCID 2733933—
ReactantHCID 85854015HCID 85854015—
ProductHCID 44217313HCID 442173138%

Reaction Conditions

Temperature130 °C

Reaction Steps

A stirred mixture of 2-chloro-6-(4-fluoro-benzyloxy)-quinoline (0.08 g, 0.4 mmol) and (R)-1-aminoindane (0.107 g, 1.00 mmol) was heated in a sealed tube for 20 h at 130° C. Purification by flash chromatography on silica gel (ethyl acetate in heptane, 0→80%) yielded the title compound as a dark oil (9 mg, 8%), MS 385.6 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188284B2
Source datasetuspto-grants-2012_05
ORD IDord-dcd1f385feac4e2d9b2659417a084765
Source noteuspto-grants-2012_05