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HRID 25528作成日:2026年10月23日

4-Nitrobenzaldehyde → [5-(5,6-Difluoro-1H-indol-2-yl)-2-methoxy-phenyl]-4nitro-benzylamine

https://huagongshe.com/ja/reaction/25528

反応式

関与物質

役割名称HCID仕込み量
反応物4-NitrobenzaldehydeHCID 541—
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]-4nitro-benzylamineHCID 1027290555%

反応手順

4-Nitrobenzaldehyde (0.3 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 (0.46 g, 2.2 mmol) was added in one portion, and the resulting homogeneous solution was stirred at room temperature for 6 days. Saturated aqueous sodium bicarbonate solution (100 mL) was added, and the mixture was stirred for 2 hours. The mixture was shaken; the organic layer was separated and dried over Na2SO4. The solvent was evaporated to give a red solid. Recrystallization from methanol gave the product (450 mg), mp 181-182° 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-e5680f1e35684a7e8e714f326cfd5c99
出典メモuspto-grants-2005_02