2-(2-Dimethylamino-ethoxy)-benzoic acid → 5-{2-[2-(N,N-dimethylamino)ethyl]oxy-phenyl}-3-(4-hydroxy-phenyl)-1,2,4-oxadiazole

反応式

[CH3:1][N:2]([CH2:4][CH2:5][O:6][C:7]1[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=1[C:9]([OH:11])=O)[CH3:3].Cl.[NH:17]=[C:18]=[NH:19].[OH:20][C:21]1[C:29]2N=NN[C:25]=2[CH:24]=[CH:23][CH:22]=1>CN(C=O)C>[CH3:3][N:2]([CH2:4][CH2:5][O:6][C:7]1[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=1[C:9]1[O:11][N:19]=[C:18]([C:24]2[CH:25]=[CH:29][C:21]([OH:20])=[CH:22][CH:23]=2)[N:17]=1)[CH3:1]

参加物

実験手順

2,45 g of 2-[2-(N,N-dimethylamino)ethyl]oxy-benzoic acid are dissolved with 1.91 g of N-ethyl-N-dimethylaminopropyl)carbodiimide hydrochloride and catalytic amounts of hydroxybenzotriazole in 50 ml of DMF. After 15 minutes 1.52 g of 4-hydroxybenzoic acid amidoxime are added and the mixture is heated for 15 minutes at 700 W in the microwave. It is concentrated by evaporation, the residue is taken up in ethyl acetate, washed with water, dried over sodium sulphate and concentrated by evaporation in vacuo. The residue is filtered over silica gel with ethanol and converted into the salt as described above. Yield: 1.1 g (29% of theory). m.p.: 170° C. (decomposition).