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HRID 264542作成日:2026年10月27日

N-(2-aminoethyl)acetamide → N-[2-(4,5-dihydro-6-methoxy-1H-benz[g]indol-1-yl)ethyl]-acetamide

https://huagongshe.com/reaction/264542

反応式

関与物質

役割名称HCID仕込み量
反応物N-(2-aminoethyl)acetamideHCID 66082—
反応物2-(2-Oxoethyl)-5-methoxy-1-tetraloneHCID 19036372—
溶媒Acetic AcidHCID 176—
生成物N-[2-(4,5-dihydro-6-methoxy-1H-benz[g]indol-1-yl)ethyl]-acetamideHCID 1903652646%

反応手順

175 mg of 2-(2-oxoethyl)-5-methoxy-1-tetralone and 144 mg of N-acetylethylenediamine were heated to reflux under argon in 4 ml of acetic acid for 1.5 hours. The solvent was removed in a vacuum. The residue was taken up in 25 ml of water and extracted several times with dichloromethane. Chromatography on 20 g of silica gel with ethyl acetate gave a greenish coloured oil. This was crystallized from toluene for purification. 91 mg (46%) of N-[2-(4,5-dihydro-6-methoxy-1H-benz[g]indol-1-yl)ethyl]-acetamide with m.p. 133° were obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05646173
出典データセットuspto-grants-1997_07
ORD IDord-6e8467599f374d0a8bc719705f2a54b4
出典メモuspto-grants-1997_07