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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1715731생성일: 2026년 10월 27일

Potassium Hydroxide → Irbesartan

https://huagongshe.com/reaction/1715731

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물Sodium HydroxideHCID 14798—
반응물5-(4'-(Bromomethyl)(1,1'-biphenyl)-2-yl)-1-trityl-1H-tetraazoleHCID 10053461—
반응물2-Butyl-1,3-diazaspiro(4.4)non-1-en-4-one hydrochlorideHCID 10176995—
촉매Tetrabutylammonium BromideHCID 74236—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물IrbesartanHCID 374992%

반응 조건

온도85 °C

반응 단계

16.4 g of sodium hydroxide dissolved in 240 ml of purified water was added to the mixture of 5-(4′-bromomethyl-biphenyl-2-yl)-1-trityl-1H-tetrazole (59.5 g) and 2n-butyl-1,3-diazaspiro (4,4) non-1-en-4-one HCl (25 g) and tetra butyl ammonium bromide (2.15 g) in toluene (250 ml). The mixture was heated to about 85° C. for about 2 hours. After reaction completion, the reaction mass was cooled to about 25° C. and the toluene layer separated. The aqueous phase was extracted with toluene (105 ml). The combined organic layer was evaporated. The residue was dissolved in acetone (208 ml) and 3N HCl was added (600 ml). The contents were stirred at room temperature until reaction completion (as monitored by TLC). After reaction completion, a solution of KOH (30.4 g) in water (208 ml) was slowly added and acetone was evaporated under reduced pressure. The precipitated trityl alcohol was filtered and washed with water (2×105 ml). The filtrate was washed with toluene and slowly acidified to pH 4 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 (2×50 ml) and dried under reduced pressure at 50-60° C. to yield irbesartan free base (92.0%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07799928B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-1c7ab24aee014bf79d437d20d7be988e
출처 메모uspto-grants-2010_09