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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922401Generated: October 30, 2026

Borane → N,N-Dimethyl-2-(6-nitro-3,4-dihydroquinolin-1(2H)-yl)ethanamine

https://huagongshe.com/reaction/1922401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoraneHCID 6331—
Reactant1-(2-(dimethylamino)ethyl)-6-nitro-3,4-dihydroquinolin-2(1H)-oneHCID 53392091—
SolventTetrahydrofuranHCID 8028—
ProductN,N-Dimethyl-2-(6-nitro-3,4-dihydroquinolin-1(2H)-yl)ethanamineHCID 5980715563.1%

Reaction Steps

A solution of 1-(2-(dimethylamino)ethyl)-6-nitro-3,4-dihydroquinolin-2(1H)-one (1.0 g, 3.80 mmol) in 10 mL THF was cooled to 0° C. and treated with a solution of 1M borane in THF (21.5 mL, 21.50 mmol). The solution was heated at reflux for 6 hours then stirred at room temperature for 1 day. After this time, the mixture was cooled to 0° C. and quenched with methanol (5 mL). The mixture was concentrated, dissolved in methanol (20 mL), stirred at room temperature for 3 days then heated at reflux for 6 hours. The reaction was concentrated and the residue was subjected to Biotage silica gel chromatography using a gradient of 1-10% 2M NH3 in MeOH/CH2Cl2 to give a viscous oil (598 mg, 63.1%). 1H-NMR (CDCl3) δ 7.96 (dd, J=2.7, 9 Hz, 1H), 7.85 (d, J=2.1 Hz, 1H), 6.48 (d, J=9 Hz, 1H), 3.50-3.43 (m, 4H), 2.78 (t, J=6.3 Hz, 2H), 2.50 (t, J=7.5 Hz, 2H), 2.29 (t, 6H), 1.99-1.94 (m, 2H). MS (ESI): 250.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173813B2
Source datasetuspto-grants-2012_05
ORD IDord-d6db54391ef548f988557479995e1bd2
Source noteuspto-grants-2012_05