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HRID 8626作成日:2026年10月24日

N-Methylhomoveratrylamine → N-[2-(3,4-Dimethoxy-phenyl)-ethyl]-4-ethoxy-N-methyl-3-(6-methyl-4-oxo-8-propyl-3,4-dihydro-imidazo[1,5-a][1,3,5]triazin-2-yl)-benzenesulfonamide

https://huagongshe.com/ja/reaction/8626

反応式

関与物質

役割名称HCID仕込み量
反応物N-MethylhomoveratrylamineHCID 77039—
反応物4-Ethoxy-3-(6-methyl-4-oxo-8-propyl-3,4-dihydro-imidazo[1,5-a][1,3,5]triazin-2-yl)-benzene-sulfonyl chlorideHCID 135424668—
溶媒DichloromethaneHCID 6344—
生成物N-[2-(3,4-Dimethoxy-phenyl)-ethyl]-4-ethoxy-N-methyl-3-(6-methyl-4-oxo-8-propyl-3,4-dihydro-imidazo[1,5-a][1,3,5]triazin-2-yl)-benzenesulfonamideHCID 135723511—

反応手順

143 mg (0.73 mmol) of N-(3,4-dimethoxyphenylethyl)-N-methylamine are added to a solution of 100 mg (0.24 mmol) of 4-ethoxy-3-(6-methyl-4-oxo-8-propyl-3,4-dihydro-imidazo[1,5-a][1,3,5]triazin-2-yl)-benzenesulfonyl chloride (example VI) in 5 ml of dichloromethane and the reaction mixture is stirred at room temperature for 2 hours. After chromatographic purification (dichloromethane/methanol=95:5), 138 mg (98%) of N-[2-(3,4-dimethoxy-phenyl)-ethyl]-4-ethoxy-N-methyl-3-(6-methyl-4-oxo-8-propyl-3,4-dihydro-imidazo[1,5-a][1,3,5]triazin-2-yl)-benzene-sulfonamide are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091203B2
出典データセットuspto-grants-2006_08
ORD IDord-936d5bb6add248b09e6db41a86e6f77c
出典メモuspto-grants-2006_08