Methylhydrazine → 4-(3-Aminooxy-propoxy)-2-hydroxy-benzoic acid methyl ester
반응식
[CH3:1][O:2][C:3](=[O:27])[C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:11][CH2:12][CH2:13][O:14][N:15]2C(=O)C3C(=CC=CC=3)C2=O)=[CH:6][C:5]=1[OH:26].CNN>>[CH3:1][O:2][C:3](=[O:27])[C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:11][CH2:12][CH2:13][O:14][NH2:15])=[CH:6][C:5]=1[OH:26]참가 물질
3
실험 절차
This compound was produced using similar methods as those used in Step 2, example 4, starting with 4-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-propoxy]-2-hydroxy-benzoic acid methyl ester (0.42 g, 1.12 mmol) and methyl hydrazine (0.087 g, 1.88 mmol). The crude material was purified by flash chromatography through silica gel using ethyl acetate/chloroform (10/90) to give 4-(3-aminooxy-propoxy)-2-hydroxy-benzoic acid methyl ester (0.26 g, 96%) as a white solid. 1H NMR (400 MHz, CDCl3); δ 7.51 (d, 1H), 6.23 (s, 1H), 6.21 (d, 1H), 3.85 (t, 2H), 3.69 (s, 3H), 3.62 (t, 2H), 1.86 (m, 2H).