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HRID 25385作成日:2026年10月25日

Pyridine → HCID 22319544、化合物

https://huagongshe.com/reaction/25385

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Benzoyl chlorideHCID 7412—
反応物3-Amino-5-nitroindazoleHCID 3136655—
溶媒WaterHCID 962—
生成物HCID 22319544HCID 22319544—

反応手順

N-(5-Nitro-1H-indazol-3-yl)benzamide can be obtained in the following way: 0.39 ml of benzoyl chloride is added dropwise to a solution, cooled to 0° C., of 0.6 g of 3-amino-5-nitro-1H-indazole and of 5 ml of pyridine. The medium is brought back to a temperature in the region of 20° C. and maintained with stirring for 18 hours. After addition of 20 ml of distilled water, the medium is extracted with 20 ml and 10 ml of ethyl acetate. The organic phases are pooled, dried over magnesium sulfate, filtered and concentrated by evaporation under reduced pressure. The residue thus obtained is purified by chromatography on a silica column with a dichloromethane/methanol (99/1 by volume) mixture as eluent. 0.9 g of N-(5-nitro-1H-indazol-3-yl)benzamide is thus obtained in the form of an orange solid melting at 231° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858638B2
出典データセットuspto-grants-2005_02
ORD IDord-b32628b6c1cb473093f6eeb51a7dbc2f
出典メモuspto-grants-2005_02