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HRID 251685作成日:2026年10月25日

Hydroxylamine → 6-(4-(((5-fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)benzamido)-N-hydroxyhexanamide

https://huagongshe.com/reaction/251685

反応式

関与物質

役割名称HCID仕込み量
反応物HydroxylamineHCID 787—
反応物TriethylamineHCID 8471—
反応物Ethyl chloroformateHCID 10928—
反応物6-(4-(((5-Fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)benzamido)hexanoic acidHCID 136387978—
溶媒DimethylformamideHCID 6228—
溶媒Sodium chloride; waterHCID 57417360—
生成物6-(4-(((5-fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)benzamido)-N-hydroxyhexanamideHCID 13638797951%

反応条件

温度0 °C

反応手順

6-(4-(((5-fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)benzamido)hexanoic acid (424 mg, 1 mmol), triethylamine (151 mg, 1.5 mmol) and 20 ml of DMF were stirred at 0° C. while ethyl chloroformate (163 mg, 1.5 mmol) was added. The mixture was stirred at 0° C. for 2 hours, and then 50% aqueous solution of hydroxylamine (1.32 g, 20 mmol) was added. The mixture was stirred for 3 hours at room temperature, and then diluted with 1000 mL of brine. The solids were collected by vacuum filtration, washed with water and dried under vacuum to give the title compound (224 mg, 51%) as a brown solid. LC-MS (m/z) 440 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07863315B2
出典データセットuspto-grants-2011_01
ORD IDord-c1f85602a9f54977a4ce57f369fab944
出典メモuspto-grants-2011_01