Benzoureas having anti-diabetic activity
A compound, phenyl technology, applied in the direction of active ingredients of heterocyclic compounds, organic chemistry, diseases, etc., can solve the problems of negative effects of lipids, inability to significantly improve lipid metabolism, weak efficacy, etc.
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[0153] The following reaction scheme examples are provided to illustrate the invention and should not be construed as limiting the invention in any way. The scope of the invention is defined by the claims.
[0154] The formulas in Table 1 further illustrate compounds that are made or can be made using the methods disclosed herein.
[0155] The synthesized compounds in Table 1 were analyzed by high pressure liquid chromatography-mass spectrometry (LC-MS) and / or proton NMR. LC-MS samples were analyzed using an Agilent 1100 Series High Pressure Liquid Chromatography coupled to a Waters MicromassZQ mass spectrometer. The column used was Waters Xterra and the compound was eluted using a gradient elution program (10% B to 100% B in 4.5 min) at a flow rate of 2.5 mL / min. Solvent A: water containing 0.06% trifluoroacetic acid. Solvent B: Acetonitrile containing 0.05% trifluoroacetic acid. Retention times are given in minutes.
[0156] Method A: XTerra MS-C18, 4.5 x 50mm, 10-100% ...
Embodiment 1
[0248]
[0249] (5R)-5-(3-{[3-(5-chloro-1,2-benzisoxazol-3-yl)-2-oxo-2,3-dihydro-1H-benzimidazole -1-yl]methyl}phenyl)-5-methyl-1,3-oxazolidine-2,4-dione:
[0250] 1 H NMR (500MHz, CDCl 3 )δ8.39(s, 1H), 8.33(brs, 1H), 7.92(d, 1H), 7.71(s, 1H), 7.61(s, 2H), 7.58(d, 1H), 7.42(m, 2H ), 7.21(d, 2H), 7.02(d, 1H), 5.23(dd, 2H), 1.99(s, 3H).
Embodiment 2
[0252]
[0253] (5R)-5-(4-chloro-3-{[3-(6-methoxy-1,2-benzisoxazol-3-yl)-2-oxo-6-(trifluoromethane Base)-2,3-dihydro-1H-benzimidazol-1-yl]methyl}phenyl)-5-methyl-1,3-oxazolidine-2,4-dione:
[0254] 1 H NMR (500MHz, CDCl 3 )δ8.14(d, 1H), 8.02(d, 1H), 7.67(s, 1H), 7.57(s, 1H), 7.52(d, 1H), 7.26(m, 2H), 7.09(s, 1H ), 7.06(d, 1H), 5.38(s, 2H), 3.98(s, 3H), 1.83(s, 3H).
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