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HRID 748658作成日:2026年10月27日

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

https://huagongshe.com/reaction/748658

反応式

関与物質

役割名称HCID仕込み量
反応物4-Iodo-1-tritylimidazoleHCID 618252—
反応物1-(Isoquinolin-1-yl)ethan-1-oneHCID 13157214—
反応物HCID 178418443HCID 178418443—
溶媒DichloromethaneHCID 6344—
生成物1-isoquinolin-1-yl-1-(1-trityl-1H-imidazol-4-yl)-ethanolHCID 59751483—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07399868B2
出典データセットuspto-grants-2008_07
ORD IDord-233ecd94c5474dd7a7ef2c8171474ec3
出典メモuspto-grants-2008_07