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HRID 1988373作成日:2026年10月27日

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 2-Chloro-(1-hydroxy-cycloheptylmethyl)-5-(5-methyl-1H-pyrazol-3-yl)-benzamide

https://huagongshe.com/reaction/1988373

反応式

関与物質

役割名称HCID仕込み量
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物1-(Aminomethyl)cycloheptanol hydrochlorideHCID 18438647—
反応物2-chloro-5-(5-methyl-1H-pyrazol-3-yl)benzoic acidHCID 18438660—
溶媒DimethylformamideHCID 6228—
生成物2-Chloro-(1-hydroxy-cycloheptylmethyl)-5-(5-methyl-1H-pyrazol-3-yl)-benzamideHCID 6905536826.2%

反応手順

To a solution of 2-chloro-5-(5-methyl-1H-pyrazol-3-yl)-benzoic acid (100 mg, 0.422 mmol) in DMF (10 mL) was added 1-hydroxybenzotriazole (85 mg, 0.63 mmol), polystyrene supported 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (1.24 g, 1.27 mmol) and 1-aminomethyl-cycloheptanol hydrochloride (113.4 mg, 0.633 mmol). The mixture was stirred at room temperature for 15 minutes, then polystyrene supported N,N-dimethylaminopyridine (0.64 g, 0.93 mmol) was added and the mixture was stirred at room temperature for 16 h. The mixture was filtered through a glass frit, and the residue was washed thoroughly with methanol. The filtrate was concentrated to dryness in vacuo. The residue was purified by reverse phase chromatography to afford the title compound as a white solid (40 mg). LC/MS (M/z): 362.5 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07553972B2
出典データセットuspto-grants-2009_06
ORD IDord-a5f3f25d0a094dceaddfb8ddf91ae2d4
出典メモuspto-grants-2009_06