돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1715733생성일: 2026년 10월 26일

Toluene → Irbesartan

https://huagongshe.com/reaction/1715733

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Potassium HydroxideHCID 14797—
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 hydrogen sulfateHCID 94433—
용매WaterHCID 962—
생성물IrbesartanHCID 374984%

반응 조건

온도90 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07799928B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-d927150c0f89466487c75930c35a7c6b
출처 메모uspto-grants-2010_09