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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 748658생성일: 2026년 10월 25일

4-Iodo-1-tritylimidazole → 1-isoquinolin-1-yl-1-(1-trityl-1H-imidazol-4-yl)-ethanol

https://huagongshe.com/reaction/748658

반응식

참여 물질

역할이름HCID투입량
반응물4-Iodo-1-tritylimidazoleHCID 618252—
반응물1-(Isoquinolin-1-yl)ethan-1-oneHCID 13157214—
반응물HCID 178418443HCID 178418443—
용매DichloromethaneHCID 6344—
생성물1-isoquinolin-1-yl-1-(1-trityl-1H-imidazol-4-yl)-ethanolHCID 59751483—

반응 단계

A mixture of 4-iodo-1-tritylimidazole (commercially available) (15.5 g, 35.4 mmol) in dichloromethane (80 mL) at 20° C. was treated with ethyl magnesium bromide (12.0 mL, 36 mmol, 3M in ether) and allowed to react for 1 h. A solution of 1-isoquinolin-1-yl-ethanone (Intermediate H2) (3.65 g, 21.3 mmol) in dichloromethane (20 mL) was added via addition funnel at 20° C. and stirred for 16 h. The mixture was quenched with sat. ammonium chloride (100 mL) and diluted with dichloromethane. The residue was isolated in an aqueous workup. The product was extracted with CH2Cl2 and purified by chromatography on silica gel with 5% NH3-MeOH: CH2Cl2 to give 1-isoquinolin-1-yl-1-(1-trityl-1H-imidazol-4-yl)-ethanol (Intermediate H3) as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07399868B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-233ecd94c5474dd7a7ef2c8171474ec3
출처 메모uspto-grants-2008_07