Preparation method of terbutaline
A technology for terbutaline and a compound, which is applied in the field of preparation of terbutaline, can solve the problems of expensive and unobtainable raw materials, lack of economy, long synthesis route and the like, and achieves easy control of the reaction process, shortened reaction steps and mild reaction conditions. Effect
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Embodiment 1
[0063] Example 1 Preparation of compound 1b (3,5-dihydroxybenzeneboronic acid pinacol ester)
Embodiment 1-1
[0065]
[0066] Under nitrogen protection, 19.0g 5-bromoresorcinol, 28.0g biboronic acid pinacol ester, 30.0g potassium acetate and 2.2g Pd(dppf)Cl were mixed 2 Dissolve in 150 mL of 1,4-dioxane, heat to 100 °C, and monitor by TLC to detect no 5-bromoresorcinol. The mixture was cooled to room temperature, diluted with toluene, filtered to remove insolubles, the filtrate was washed with an equal volume of water, the organic phase was separated, dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated to dryness to obtain 21.1 g of compound 1b with a yield of 89.0%, HPLC purity 95.8%.
Embodiment 1-2
[0068]
[0069] Under nitrogen protection, 14.0g 5-chlororesorcinol, 28.0g biboronic acid pinacol ester, 25.0g sodium acetate and 2.2g Pd(dppf)Cl were mixed 2 Dissolved in 150 mL DMSO, heated to 120°C, and monitored by TLC for the absence of 5-chlororesorcinol. It was cooled to room temperature, diluted with toluene, filtered to remove insolubles, the filtrate was washed with an equal volume of water, the organic phase was separated, dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated to dryness to obtain 19.5 g of compound 1b with a yield of 82.3%. HPLC purity 95.6%.
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