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HRID 230119作成日:2026年10月26日

Triethylamine → N-(2,6-dimethylphenyl)-2-[4-(4-oxo-4-phenylbutyl)piperazin-1-yl]acetamide

https://huagongshe.com/reaction/230119

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-ChlorobutyrophenoneHCID 253533—
反応物Cvt-2738HCID 2608606—
溶媒EthanolHCID 702—
生成物N-(2,6-dimethylphenyl)-2-[4-(4-oxo-4-phenylbutyl)piperazin-1-yl]acetamideHCID 18452749—

反応手順

A mixture of N-(2,6-dimethylphenyl)-2-piperazinylacetamide (4) (100 mg, 0.4 mmol), 4-chloro-1-phenylbutan-1-one (12) (100 mg, 0.55 mmol), and triethylamine (0.4 mL) in ethanol (3 mL) was heated at reflux for 16 hours. Ethanol was removed under reduced pressure and the residue was purified by preparative TLC using 10% methanol in dichloromethane as mobile phase to afford N-(2,6-dimethylphenyl)-2-[4-(4-oxo-4-phenylbutyl)piperazin-1-yl]acetamide, a compound of formula (16).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07566717B2
出典データセットuspto-grants-2009_07
ORD IDord-6408f689aac34bd39bd9df7b6be3b91e
出典メモuspto-grants-2009_07