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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669016Generated: October 30, 2026

(2-Aminoethyl)dipropylamine → N1-(1-Oxido-7,8-dihydro-6H-indeno[5,6-e][1,2,4]triazin-3-yl)-N2,N2-dipropyl-1,2-ethanediamine

https://huagongshe.com/reaction/1669016

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Aminoethyl)dipropylamineHCID 5151220—
Reactant3-Chloro-7,8-dihydro-6H-indeno[5,6-e][1,2,4]triazine 1-OxideHCID 16081320—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductN1-(1-Oxido-7,8-dihydro-6H-indeno[5,6-e][1,2,4]triazin-3-yl)-N2,N2-dipropyl-1,2-ethanediamineHCID 1195093875.9%

Reaction Steps

N1,N1-Dipropyl-1,2-ethanediamine (297) (0.27 g, 1.9 mmol) was added to a stirred solution of chloride 21 (298 mg, 1.3 mmol) in DME (50 mL) and the solution stirred at reflux temperature for 2 h. The solvent was evaporated and the residue partitioned between DCM (100 mL) and dilute aqueous NH3 solution (50 mL). The organic fraction was dried and the solvent evaporated. The residue was purified by chromatography, eluting with a gradient (0-10%) of MeOH/DCM, to give 1-oxide 28 (325 mg, 74%) as a yellow powder: mp (MeOH/EtOAc) 95-97° C.; 1H NMR δ 8.07 (s, 1H, H-9), 7.39 (s, 1H, H-5), 5.80 (br s, 1H, NH), 3.46-3.53 (m, 2H, CH2N), 2.96-3.03 (m, 4H, 2×CH2N), 2.68 (dd, J=6.0, 5.8 Hz, 2H, CH2N), 2.38-2.45 (m, 4H, H-6, H-8), 2.10-2.18 (m, 2H, H-7), 1.41-1.51 (m, 4H, 2×CH2), 0.87 (t, J=7.1 Hz, 6H, 2×CH3); 13C NMR δ 158.7, 154.4, 148.8, 143.0, 129.8, 120.5, 114.7, 55.9 (2), 52.6, 38.9, 31.1, 32.3, 25.7, 20.3 (2), 11.9 (2). Anal. calcd for C18H27N5O: C, 65.6; H, 8.3; N, 21.3. Found: C, 65.4; H, 8.4; N, 21.3%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989451B2
Source datasetuspto-grants-2011_08
ORD IDord-ae2bed47e6b041a684cf5b596e2c33bd
Source noteuspto-grants-2011_08