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HRID 74315作成日:2026年10月26日

Propylamine → 5-(5-Chlorobenzoxazol-2-yl)-2-n-propylaminoaniline

https://huagongshe.com/reaction/74315

反応式

関与物質

役割名称HCID仕込み量
反応物PropylamineHCID 7852—
反応物TriethylamineHCID 8471—
反応物5-Chloro-2-(2-fluoronitrobenzen-5-yl)benzoxazoleHCID 67497553—
反応物HCID 178418361HCID 178418361—
触媒HCID 178418390HCID 178418390—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物5-(5-Chlorobenzoxazol-2-yl)-2-n-propylaminoanilineHCID 6749865797%

反応手順

To a suspension of 5-chloro-2-(2-fluoronitrobenzen-5-yl)benzoxazole (see Working Example 100-1) (1.5 g, 5.13 mmol) in acetonitrile (10 mL) was added triethylamine (779 mg, 7.70 mmol) and propylamine (364 mg, 6.16 mmol), and this was heated to reflux for 4 hours. After the reaction was complete, this was cooled to room temperature, water was added, and the precipitated crystals were filtered, washed with water and then dried. To a solution of the crystals obtained in ethanol/tetrahydrofuran (1:2, 15 mL) was added 10% palladium-carbon (200 mg). A hydrogen atmosphere was substituted in the flask, and this was stirred at room temperature for 18 hours. After the reaction was finished, this was filtered through Celite, and the filtrate was concentrated to yield the title compound (1.5 g, 97% yield) as orange crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829035B2
出典データセットuspto-grants-2014_09
ORD IDord-1f02076f3e574d15a642b8b62727a875
出典メモuspto-grants-2014_09