5-[2-Hydroxy-3-(isopropylamino)propoxy]benzofuran derivatives and their application
A technology of isopropylamino group and benzofuran, which is applied in the field of medicine, can solve the problems of different side effects of antihypertensive drugs, and achieve the effects of novel structure type, good application value, and good development and application prospects
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Embodiment 1
[0036] Example 1: Preparation of 2-benzoyl-3-methyl-5-[2-hydroxy-3-(isopropylamino)propoxy]benzofuran (XLY-A39)
[0037] Step A: Preparation of 2'-Hydroxy-5'-Benzyloxyacetophenone
[0038] Put 2',5'-dihydroxyacetophenone (7.60g, 0.05mol), anhydrous potassium carbonate (8.00g, 0.06mol), potassium iodide (1.00g, 0.006mol), and 100mL acetone in a 250mL eggplant-shaped flask , stir well at room temperature. After diluting benzyl chloride (7.87g, 0.06mol) with 10mL of acetone, it was dropped into the reaction solution at a constant speed, and the dropwise addition was completed in about 10 minutes. The reaction was heated to reflux for 6 h, and the reaction was complete as monitored by TLC. After the reaction was completed, it was cooled to room temperature, and the organic solvent was distilled off under reduced pressure to obtain yellow crystals. 50 mL of ethanol was recrystallized to obtain 9.84 g of yellow crystals with a yield of 81.3%. m.p:60.5-63.2℃; EI-MS:243.0([M+H] +...
Embodiment 2
[0047] Example 2: Preparation of 2-(4-methylbenzoyl)-3-methyl-5-[2-hydroxyl-3-(isopropylamino)propoxy]benzofuran hydrochloride (XLY- 01)
[0048] 2-(4-methylbenzoyl)-3-methyl-5-[2-hydroxy-3-(isopropylamino)propoxy]benzofuran (XLY-A39) (0.50g, 1.31mmol ) was dissolved in 10mL of dichloromethane, and a sufficient amount of hydrogen chloride gas was passed into it. After all the salts were formed, the dichloromethane was distilled off under reduced pressure, and 3mL of ether was added to solidify and precipitate a yellow solid. Suction filtration, washing and filtration with a small amount of ethyl acetate The cake was dried to obtain 0.55 g of a yellow powdery solid, with a yield of 100%. m.p:152.5-154.0℃;IR:3342.9,3178.5,2977.0,2944.3,2784.1,2724.1,2459.3,2425.4,1628.7,1608.2,1548.2,1451.6,1431.2,1385.6,1364.2,1311.0,1287.7,1265.1,1235.8,1203.0,1184.9 , 1101.4.
Embodiment 3
[0049] Embodiment 3: Preparation of 2-(4-methylbenzoyl)-3-methyl-5-[2-hydroxyl-3-(isopropylamino)propoxy]benzofuran p-toluenesulfonate ( XLY-02)
[0050] Referring to the preparation method of Example 2, 0.60 g of white solid was obtained with a yield of 82.2%. m.p: 176.2.0-178.0℃; IR: 3334.9, 3026.9, 2921.1, 2856.4, 1642.3, 1607.4, 1566.2, 1467.1, 1452.8, 1377.1, 1328.6, 1294.5, 1236.0, 1214.5, 11103.1, 11027.6,
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