Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931482Generated: November 3, 2026

(R)-(-)-1-Aminoindan → (6-nitro-quinolin-2-yl)-(R)-indan-1-yl-amine

https://huagongshe.com/reaction/1931482

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-(-)-1-AminoindanHCID 2733933—
Reactant2-Chloro-6-nitroquinolineHCID 10921723—
Product(6-nitro-quinolin-2-yl)-(R)-indan-1-yl-amineHCID 5786096547%

Reaction Conditions

Temperature125 °C

Reaction Steps

A stirred mixture of 2-chloro-6-nitro-quinoline (2.2 g, 11 mmol) and (R)-1-aminoindane (2.8 g, 21 mmol) was heated in a sealed tube for 20 h at 125° C. Purification by flash chromatography on silica gel (ethyl acetate/heptane 0:1=>3:7) yielded (6-nitro-quinolin-2-yl)-(R)-indan-1-yl-amine as a brownish solid (1.5 g, 47%), MS 306.5 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188284B2
Source datasetuspto-grants-2012_05
ORD IDord-431c548139114268a2a4b336e057ab87
Source noteuspto-grants-2012_05