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HRID 1715733作成日:2026年10月27日

Toluene → Irbesartan

https://huagongshe.com/reaction/1715733

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Potassium HydroxideHCID 14797—
反応物5-(4'-(Bromomethyl)(1,1'-biphenyl)-2-yl)-1-trityl-1H-tetraazoleHCID 10053461—
反応物2-Butyl-1,3-diazaspiro(4.4)non-1-en-4-one hydrochlorideHCID 10176995—
触媒Tetrabutylammonium hydrogen sulfateHCID 94433—
溶媒WaterHCID 962—
生成物IrbesartanHCID 374984%

反応条件

温度90 °C

反応手順

5-(4′-bromomethyl-biphenyl-2-yl)-1-trityl-1H-tetrazole (24.6 g) was charged to toluene (240 ml). To this, a solution of KOH (10.4 g), 2n-butyl-1,3-diazaspiro (4,4) non-1-en-4 one HCl (12.0 g) and Bu4NHSO4 (1.8 g) in water (40 ml) was added. The two-phase mixture was then heated to 90° C. for 90 minutes under vigorous stirring. The reaction mixture was cooled to room temperature. The toluene layer was separated and the aqueous phase was extracted with toluene (50 ml). The combined organic layer was evaporated. The residue was dissolved in acetone (100 ml) and 3N HCl (52 ml) and stirred at room temperature (TLC monitoring). A solution of KOH (14.6 g) in water (100 ml) was slowly added and acetone was evaporated under reduced pressure. The precipitated trityl alcohol was filtered and washed with water (2×50 ml). The filtrate was washed with toluene and slowly acidified to pH 4.0 with 3 N HCl. The suspension was cooled to 0-4° C., stirred for an additional 30 minutes and filtered. The cake was washed with cold isopropanol (2×25 ml) and dried under reduced pressure at 50-60° C. to yield irbesartan free base (84%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07799928B2
出典データセットuspto-grants-2010_09
ORD IDord-d927150c0f89466487c75930c35a7c6b
出典メモuspto-grants-2010_09