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HRID 32177作成日:2026年10月24日

Tri-tert-butylphosphine tetrafluoroborate → 1-[4-Azetidin-1-yl-2-(4,4-dimethylcyclohexyl)phenyl]-4-butylpiperazine

https://huagongshe.com/ja/reaction/32177

反応式

関与物質

役割名称HCID仕込み量
反応物Tri-tert-butylphosphine tetrafluoroborateHCID 2734635—
反応物Azetidine hydrochlorideHCID 12308726—
反応物1-[4-Bromo-2-(4,4-dimethylcyclohexyl)phenyl]-4-butylpiperazineHCID 23141738—
反応物Sodium t-butoxideHCID 23676156—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒O-XyleneHCID 7237—
溶媒Ethyl AcetateHCID 8857—
生成物1-[4-Azetidin-1-yl-2-(4,4-dimethylcyclohexyl)phenyl]-4-butylpiperazineHCID 59769431—

反応条件

温度100 °C

反応手順

A mixture of 1-[4-bromo-2-(4,4-dimethylcyclohexyl)phenyl]-4-butylpiperazine (50 mg, 0.123 mmol) produced in Example (57b), azetidine hydrochloride (17 mg, 0.185 mmol), sodium t-butoxide (47 mg, 0.492 mmol), palladium(II) acetate (3 mg, 0.0123 mmol), tri-t-butylphosphonium tetrafluoroborate (11 mg, 0.0369 mmol) and xylene (1 mL) was stirred for 3 hours at an external temperature of 100° C. Water was added to the reaction mixture and extraction was performed with ethyl acetate. The separated organic layer was filtered through Celite. The solvent was distilled off by nitrogen stream to the filtrate. The resultant residue was purified by NH silica gel column chromatography (ethyl acetate/hexane) to give 1-[4-azetidin-1-yl-2-(4,4-dimethylcyclohexyl)phenyl]-4-butylpiperazine as a colorless solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425554B2
出典データセットuspto-grants-2008_09
ORD IDord-33f191f7e03346e3b882e7d82f26d813
出典メモuspto-grants-2008_09