Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419337Generated: October 29, 2026

Dimethylamine → 4-{5-[(Dimethylamino)methyl]-1,3,4-oxadiazol-2-yl}-2-(methyloxy)aniline

https://huagongshe.com/reaction/419337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(Chloromethyl)-5-[3-(methyloxy)-4-nitrophenyl]-1,3,4-oxadiazoleHCID 59452661—
Solvent1,4-DioxaneHCID 31275—
Product4-{5-[(Dimethylamino)methyl]-1,3,4-oxadiazol-2-yl}-2-(methyloxy)anilineHCID 5945291089.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To 2-(chloromethyl)-5-[3-(methyloxy)-4-nitrophenyl]-1,3,4-oxadiazole (0.399 g, 1.48 mmol) in dioxane (10 mL) was added dimethylamine (1.87 mL, 40% weight in H2O, 14.8 mmol). The reaction was heated at 60° C. overnight. The reaction was poured into half saturated NaHCO3, extracted with DCM and EtOAc, dried (MgSO4) and concentrated. The residue was taken up in EtOAc (20 mL) and Pd on carbon was added in one portion. The mixture was stirred at rt under H2 (1 atm.) until complete by TLC. The reaction was filtered through Celite® and concentrated to provide the title compound of step D (0.326 g, 1.32 mmol, 89% over two steps). 1H NMR (400 MHz, DMSO-d6) δ ppm 2.18-2.23 (m, 6H), 3.67-3.72 (m, 2H), 3.76-3.82 (m, 3H), 5.47-5.56 (m, 2H), 6.64-6.72 (m, 1H), 7.25 (d, J=2.0 Hz, 1H), 7.30 (dt, J=8.1, 2.1 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-32accc09dc514616b7a46a271dd2feb4
Source noteuspto-grants-2012_01