Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669165Generated: November 1, 2026

N,N-Dimethylethylenediamine → HCID 25138705, compound

https://huagongshe.com/reaction/1669165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylethylenediamineHCID 66053—
ReactantHCID 25139756HCID 25139756—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 25138705HCID 2513870588%

Reaction Steps

N,N-Dimethyl-1,2-ethanediamine (0.52 mL, 4.8 mmol) was added to a stirred solution of chloride 222 (359 mg, 1.6 mmol) in DME (40 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 (0-15%) of MeOH/DCM, to give 1-oxide 223 (390 mg, 88%) as a yellow solid: mp (MeOH/DCM) 192-194° C.; 1H NMR δ 7.45 (s, 1H, H-9), 7.35 (br s, 1H, NH), 6.96 (s, 1H, H-5), 6.23 (s, 2H, H-7), 3.35-3.39 (m, 2H, CH2N), 2.42 (t, J=6.7 Hz, 2H, CH2N), 2.18 [s, 6H, N(CH3)2]; 13C NMR δ 158.9, 155.2, 148.7, 146.9, 125.3, 103.2, 101.6, 95.9, 57.8, 45.2 (2), 38.6. Anal. calcd for C12H15N5O3: C, 52.0; H, 5.5; N, 25.3. Found: C, 52.1; H, 5.5; N, 25.3%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989451B2
Source datasetuspto-grants-2011_08
ORD IDord-f711b4df80b8425e8595039b82de9008
Source noteuspto-grants-2011_08