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HRID 895515作成日:2026年10月26日

Sodium Sulfate → 1-Propyl-2-{[2-(2-fluoropyrid-6-yl)-1H-imidazol-1-yl]methyl}-5-cyano-1H-benzimidazole

https://huagongshe.com/reaction/895515

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium SulfateHCID 24436—
反応物TrimethylaluminumHCID 16682925—
反応物3-Amino-4-(propylamino)benzonitrileHCID 22380299—
反応物[2-(2-Fluoropyridin-6-yl)-imidazol-1-yl]acetic acid methyl esterHCID 68499258—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物1-Propyl-2-{[2-(2-fluoropyrid-6-yl)-1H-imidazol-1-yl]methyl}-5-cyano-1H-benzimidazoleHCID 984180636.8%

反応手順

Trimethylaluminum (0.54 mL of 2.0M in toluene, 1.09mmol) is added dropwise to a solution of 3-Amino-4-propylaminobenzonitrile (152 mg; 0.87 mmol) in dichloromethane (10 mL), and the mixture was stirred at room temperature for 1 hr. A solution of [2-(2-Fluoropyridin-6-yl)-imidazol-1-yl]acetic acid methyl ester (102 mg; 0.43 mmol) in dichloromethane (5 mL) is added all at once, and the mixture heated at reflux for 16 hr. The brown solution is cooled to room temperature and treated dropwise with methanol (1 mL) then water (2 mL) and stirred at room temperature for 15 min. Anhydrous sodium sulfate is added until the gel becomes solid, the mixture is diluted with dichloromethane (100 mL) and filtered through celite. The filtrate is concentrated to give a brown oil which is dissolved in acetic acid (7 mL) and heated at 100° for 72 hr. The mixture is cooled to room temperature and concentrated. The residue is dissolved in ethyl acetate (15 mL), washed with saturated aqueous NaHCO3 (1×50 mL), then brine (1×50 mL), dried (MgSO4), and concentrated, and the residue purified by preparative thin layer chromatography to give 1-n-Propyl-2-{[2-(2-fluoropyrid-6-yl)-1H-imidazol-1-yl]methyl}-5-cyano-1H-benzimidazole as a light brown semi-solid (57 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06916819B2
出典データセットuspto-grants-2005_07
ORD IDord-9062e89d56914e4cb5e380926c11f13a
出典メモuspto-grants-2005_07