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HRID 25532作成日:2026年10月24日

m-Formylbenzonitrile → [5-(5,6-Difluoro-1H-indol-2yl)-2-methoxy-phenyl]-(3-cyano-benzyl)-amine

https://huagongshe.com/ja/reaction/25532

反応式

関与物質

役割名称HCID仕込み量
反応物m-FormylbenzonitrileHCID 90670—
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-2yl)-2-methoxy-phenyl]-(3-cyano-benzyl)-amineHCID 1029368364.2%

反応手順

3-Cyanobenzaldehyde (0.262 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, 2.0 mmol) was added in one portion, and the resulting homogeneous solution stirred at room temperature for 3 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 Na2S4. The solvent was evaporated to give a white solid. Recrystallization from methanol gave the product (500 mg), mp 154-155° 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-f64a7462a3de4a72833949b2f318e2f3
出典メモuspto-grants-2005_02