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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669014Generated: October 30, 2026

N,N-Diethylethylenediamine → HCID 11950762, compound

https://huagongshe.com/reaction/1669014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DiethylethylenediamineHCID 60993—
Reactant3-Chloro-7,8-dihydro-6H-indeno[5,6-e][1,2,4]triazine 1-OxideHCID 16081320—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 11950762HCID 1195076296.2%

Reaction Steps

N1,N1-Diethyl-1,2-ethanediamine (0.50 mL, 3.5 mmol) was added to a stirred solution of chloride 21 (314 mg, 1.4 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 26 (406 mg, 95%) as a yellow solid: mp (MeOH/EtOAc) 109-112° C.; 1H NMR δ 7.93 (s, 1H, H-9), 7.31 (s, 1H, H-5), 7.14 (br s, 1H, NH), 3.97-4.03 (m, 2H, CH2N), 3.42-3.46 (m, 2H, CH2N), 3.25-3.33 (m, 4H, 2×CH2N), 2.19-2.29 (m, 4H, H-6, H-8), 2.08-2.14 (m, 2H, H-7), 1.45 (t, J=7.3 Hz, 6H, 2×CH3); 13C NMR δ 158.2, 154.6, 148.4, 143.7, 129.8, 120.7, 114.4, 50.8, 47.7 (2), 36.3, 33.1, 32.3, 25.7, 8.8 (2). Anal. calcd for C16H23N5O: C, 63.8; H, 7.7; N, 23.2. Found: C, 63.9; H, 7.7; N, 23.3%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989451B2
Source datasetuspto-grants-2011_08
ORD IDord-72eb64863617497c90e9a96ad0d6c7e8
Source noteuspto-grants-2011_08