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HRID 573369作成日:2026年10月26日

Dimethylformamide → N3-(6-nitro-1,3-benzothiazol-2-yl)-2-(4-methoxyanilino)nicotinamide

https://huagongshe.com/reaction/573369

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物2-Amino-6-nitrobenzothiazoleHCID 22704—
反応物2-(4-Methoxy-phenylamino)-nicotinic acidHCID 748369—
生成物N3-(6-nitro-1,3-benzothiazol-2-yl)-2-(4-methoxyanilino)nicotinamideHCID 57394067—

反応条件

温度27 °C

反応手順

To a stirred solution of 2-(4-methoxy phenylamino)nicotinic acid (29, 244 mg 1 mmol) in dry DMF (10 mL) hydroxy benzotriazole HOBt (1.2 mmol) were added at 0° C. After 10 min 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDCI) (1.2 mmol) was added and finally 2-amino-6-nitrobenzothiazole (37, 137 mg, 0.7 mmol) were added, then the resulting mixture was stirred at room temperature (27° C.) for 8-10 h and then the reaction mixture was quenched with NaHCO3 and extracted in ethyl acetate (4×25 mL) from the ice cold aqueous layer and dried over anhydrous Na2SO4. The resulting product (5) was purified by column chromatography employing EtOAc/Hexane as an eluent.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09029553B2
出典データセットuspto-grants-2015_05
ORD IDord-82b42c78ccde425e9db9537b997fb2f6
出典メモuspto-grants-2015_05