Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669174Generated: October 30, 2026

N,N-Dimethylethylenediamine → N1,N1-Dimethyl-N2-(1-oxido-7,8-dihydro-6H-chromeno[6,7-e][1,2,4]triazin-3-yl)-1,2-ethanediamine

https://huagongshe.com/reaction/1669174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylethylenediamineHCID 66053—
Reactant3-Chloro-7,8-dihydro-6H-chromeno[6,7-e][1,2,4]triazine 1-OxideHCID 25139884—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductN1,N1-Dimethyl-N2-(1-oxido-7,8-dihydro-6H-chromeno[6,7-e][1,2,4]triazin-3-yl)-1,2-ethanediamineHCID 2513870884.7%

Reaction Steps

N,N-Dimethyl-1,2-ethanediamine (0.47 mL, 4.3 mmol) was added to a stirred solution of chloride 240 (341 mg, 1.4 mmol) in DME (30 mL) and the solution stirred at reflux temperature for 4 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 241 (343 mg, 83%) as a yellow solid: mp (MeOH/EtOAc) 150-152° C.; 1H NMR δ 7.58 (s, 1H, H-10), 7.30 (s, 1H, H-5), 5.79 (br s, 1H, NH), 4.25 (br dd, J=5.3, 5.2 Hz, 2H, H-8), 3.51-3.56 (m, 2H, CH2N), 2.96 (br t, J=6.0 Hz, 2H, H-6), 2.60 (br t, J=6.0 Hz, 2H, CH2N), 2.31 [s, 6H, N(CH3)2], 2.02-2.09 (m, 2H, H-7); 13C NMR δ 158.0, 152.9, 143.6, 135.1, 130.0, 126.1, 104.3, 66.9, 57.6, 45.0 (2), 38.7, 25.9, 21.7. Anal. calcd for C14H19N5O2.½H2O: C, 57.2; H, 6.7; N, 23.8. Found: C, 57.1; H, 6.5; N, 23.9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989451B2
Source datasetuspto-grants-2011_08
ORD IDord-19304c818c2845bcab30da494ee195f0
Source noteuspto-grants-2011_08