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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822861Generated: October 26, 2026

(+-)-1-Aminoindan → 4-(2,3-Dihydro-1H-inden-1-ylamino)-6,7-dimethoxy-3-quinoline carboxamide

https://huagongshe.com/reaction/1822861

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+-)-1-AminoindanHCID 123445—
Reactant4-Chloro-6,7-dimethoxyquinoline-3-carboxamideHCID 22170204—
SolventDimethylformamideHCID 6228—
Product4-(2,3-Dihydro-1H-inden-1-ylamino)-6,7-dimethoxy-3-quinoline carboxamideHCID 2217021370%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-chloro-6,7-dimethoxy-3-quinolinecarboxamide (0.066 g, 0.25 mmol), 1-aminoindan (0.66 mg, 0.50 mmol), 2-butanole (2 ml), DMF (2 ml) was heated for 48 h at 100° C. After cooling, the solution was reduced by evaporation. The residue was dissolved in water (3 ml) and treated with aqueous ammonia. The solid product was fitered off washed with water air dried for 0.5 h, washed again with heptane and dried. The residue was purified by chromatography on silica (CH2Cl2/MeOH) to give 63 mg, (70%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07037925B2
Source datasetuspto-grants-2006_05
ORD IDord-8a430e7f67c14668958396ca8749f8c8
Source noteuspto-grants-2006_05