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HRID 25530作成日:2026年10月24日

4-Hydroxy-3-nitrobenzaldehyde → [5-(5,6-Difluoro-1H-indol-2-yl)-2-methoxy-phenyl](4-hydroxy-3-nitro-benzyl)-amine

https://huagongshe.com/ja/reaction/25530

反応式

関与物質

役割名称HCID仕込み量
反応物4-Hydroxy-3-nitrobenzaldehydeHCID 18169—
反応物Sodium BicarbonateHCID 516892—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物5-(5,6-difluoro1H-indol-2-yl)-2-methoxy-phenylamineHCID 9943439—
溶媒Acetic AcidHCID 176—
溶媒DichloromethaneHCID 6344—
生成物[5-(5,6-Difluoro-1H-indol-2-yl)-2-methoxy-phenyl](4-hydroxy-3-nitro-benzyl)-amineHCID 1018073935.3%

反応手順

4-Hydroxy-3-nitrobenzaldehyde (0.334 g, 2.0 mmol) was added to a stirred mixture of 5-(5,6-difluoro-1H-indol-2-yl)-2-methoxy-phenylamine (0.548 g, 2.0 mmol) in methylene chloride (125 mL), followed by acetic acid (0.2 g). The resulting mixture was stirred at room temperature for 1 hour. Sodium triacetoxyborohydride (0.47 g, 2.2 mmol) was added in one portion, and the resulting homogeneous solution stirred at room temperature for 7 days. Saturated aqueous sodium bicarbonate solution (100 mL) was added and the mixture stirred for 2 hours. The mixture was shaken, the organic layer separated and dried over Na2SO4. The solvent was evaporated to give an orange solid. Recrystallization from methanol gave the product (300 mg), mp 195-196° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858739B2
出典データセットuspto-grants-2005_02
ORD IDord-1fcdb3f9e6bb4172889cf75f84c01c6f
出典メモuspto-grants-2005_02