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HRID 576280作成日:2026年10月27日

N-Ethyl-1-naphthalenamine → Ethyl 7-bromo-3-(3-(ethyl(naphthalen-1-yl)amino)propyl)-1h-indole-2-carboxylate

https://huagongshe.com/reaction/576280

反応式

関与物質

役割名称HCID仕込み量
反応物N-Ethyl-1-naphthalenamineHCID 67043—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物ethyl 7-bromo-3-(3-oxopropyl)-1H-indole-2-carboxylateHCID 86628021—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物Ethyl 7-bromo-3-(3-(ethyl(naphthalen-1-yl)amino)propyl)-1h-indole-2-carboxylateHCID 68938635—

反応手順

To a solution of EXAMPLE 531A (130 mg) and N-ethylnaphthalen-1-amine (82 mg) in dichloromethane (3 mL) was added sodium triacetoxyborohydride (2.35 g). The mixture was stirred at room temperature overnight. After this time the mixture was diluted with ethyl acetate (1500 mL) and washed with 1N NaOH, water, brine, and dried over Na2SO4. After filtration and concentration of the filtrate, the residue was purified by flash chromatography using silica gel and eluenting with 5% ethyl acetate in hexane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09035047B2
出典データセットuspto-grants-2015_05
ORD IDord-6cd87c6596114d6ba0b4f35bd098973b
出典メモuspto-grants-2015_05