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HRID 1180008作成日:2026年10月25日

1-((4-Methoxyphenyl)methyl)piperazine → 4-(4-Methoxy-benzyl)-piperazine-1-carboxylic Acid 4-(3,3-dimethyl-butylcarbamoyl)-phenyl Ester

https://huagongshe.com/reaction/1180008

反応式

関与物質

役割名称HCID仕込み量
反応物1-((4-Methoxyphenyl)methyl)piperazineHCID 231905—
反応物4-(3,3-Dimethyl-butylcarbamoyl)-phenyl chloroformateHCID 22047873—
溶媒DichloromethaneHCID 6344—
生成物4-(4-Methoxy-benzyl)-piperazine-1-carboxylic Acid 4-(3,3-dimethyl-butylcarbamoyl)-phenyl EsterHCID 69517795—

反応手順

The title product was prepared from 1-(4-methoxy-benzyl)-piperazine (0.35 mmol) was dissolved in dichloromethane (5 ml). 4-(3,3-Dimethyl-butylcarbamoyl)-phenyl chloroformate (0.35 mmol) was added at room temperature. The reaction mixture was stirred for 16 h and evaporated to dryness and subjected to preparative HPLC (method C). (54%, colourless semicrystaline oil). HPLC-MS m/z=454.3 (M+1), Rt: 2.78 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07279470B2
出典データセットuspto-grants-2007_10
ORD IDord-2fdebb1b6d5c4eb48f6b48182cc2d98b
出典メモuspto-grants-2007_10