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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1877461생성일: 2026년 10월 25일

1-Amino-2-propanol → 4-[4-(6-fluoro-1H-benzimidazol-2-yl)-9H-carbazol-9-yl]-2-(2(R,S)-hydroxypropylamino)benzamide

https://huagongshe.com/reaction/1877461

반응식

참여 물질

역할이름HCID투입량
반응물1-Amino-2-propanolHCID 4—
반응물Hydrogen PeroxideHCID 784—
반응물Potassium CarbonateHCID 11430—
반응물Sodium HydroxideHCID 14798—
반응물2-fluoro-4-[4-(6-fluoro-1H-benzimidazol-2-yl)carbazol-9-yl]benzonitrileHCID 58338358—
용매Dimethyl SulfoxideHCID 679—
용매EthanolHCID 702—
생성물4-[4-(6-fluoro-1H-benzimidazol-2-yl)-9H-carbazol-9-yl]-2-(2(R,S)-hydroxypropylamino)benzamideHCID 58338262—

반응 단계

The process is carried out as in stage 3 of Example 3, but using 300 mg of 2-fluoro-4-[4-(6-fluoro-1H-benzimidazol-2-yl)carbazol-9-yl]benzonitrile, obtained according to stage 2 of Example 3, 296 mg of potassium carbonate and 1.073 g of 1-amino-2(R,S)-propanol in 3 ml of dimethyl sulphoxide. 1.357 ml of a 1M aqueous solution of sodium hydroxide, 1.313 ml of a 30% aqueous solution of hydrogen peroxide and 7 ml of ethanol are then added to the reaction medium. After treatment as in stage 3 of Example 3, and then purification by flash chromatography on silica gel, elution being carried out with mixtures of dichloromethane and ethanol (95/5 to 90/10 by volume), followed by crystallization from 10 ml of diisopropyl ether, 180 mg of 4-[4-(6-fluoro-1H-benzimidazol-2-yl)-9H-carbazol-9-yl]-2-(2(R,S)-hydroxypropylamino)benzamide are thus obtained in the form of a beige solid, the characteristics of which are the following:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08309721B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-7d50498b5f9f4d9ca0e9bf45f41ecf2d
출처 메모uspto-grants-2012_11