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HRID 277751作成日:2026年10月24日

tert-Butyl methyl ether → 1-(2-Methoxyphenyl)-4-[3-(cyclohexanecarbonyl)-3-(phenyl)butyl]piperazine maleate

https://huagongshe.com/ja/reaction/277751

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl methyl etherHCID 15413—
反応物Maleic AcidHCID 444266—
反応物1-Cyclohexyl-4-(4-(2-methoxyphenyl)piperazin-1-yl)-2-methyl-2-phenylbutan-1-oneHCID 9802987—
溶媒MethanolHCID 887—
生成物1-(2-Methoxyphenyl)-4-[3-(cyclohexanecarbonyl)-3-(phenyl)butyl]piperazine maleateHCID 69419574—

反応手順

1-(2-Methoxyphenyl)-4-[3-(cyclohexanecarbonyl)-3-(phenyl)butyl]piperazine (prepared directly above) was dissolved in warm methanol (50 mL) followed by addition of maleic acid (26.8 g) and MTBE (200 mL). This mixture was concentrated to a paste and then redissolved by addition of methanol (approximately 15 mL) and MTBE (200 mL). The mixture was seeded and an additional amount of MTBE (300 mL) was added once crystallization was initiated. The mixture was suction filtered, and the solid rinsed with MTBE and vacuum dried for 5 hours at 40° C. to provide the title compound (122 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06358958B2
出典データセットuspto-grants-2002_03
ORD IDord-4c784271564f4c98bec08ac2cd3593fe
出典メモuspto-grants-2002_03