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HRID 885950作成日:2026年10月26日

1-Methylpiperazine → 1-(2-Chloropyridin-4-YL)-4-methylpiperazine

https://huagongshe.com/reaction/885950

反応式

関与物質

役割名称HCID仕込み量
反応物1-MethylpiperazineHCID 53167—
反応物2-Chloro-4-iodopyridineHCID 1516511—
反応物Sodium t-butoxideHCID 23676156—
触媒Dichloro[1,1'-bis(di-tert-butylphosphino)ferrocene]palladium(II)HCID 53384307—
溶媒TolueneHCID 1140—
生成物1-(2-Chloropyridin-4-YL)-4-methylpiperazineHCID 7221889977%

反応条件

温度115 °C

反応手順

To a mixture of 2-chloro-4-iodopyridine (300 mg, 1.24 mmol) in toluene (4 mL) was added 1-methylpiperazine (0.14 mL, 1.24 mmol), sodium tert-butoxide (239 mg, 2.44 mmol), [1,1′-bis(di-tert-butylphosphino)ferrocene]palladium(II) dichloride (30 mg, 10% wt) and the suspension was heated to 115° C. under microwave irradiation for 30 minutes. The resulting mixture was concentrated in vacuo and partitioned between DCM (50 mL) and water (50 mL). The organic phase was washed with brine (50 mL), dried (MgSO4), and evaporated in vacuo to give the title compound (200 mg, 77%) as a brown oil. LCMS (ES+) 212.0 (M+H)+, RT 1.78 minutes (70% purity) (Method 2).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08242116B2
出典データセットuspto-grants-2012_08
ORD IDord-36642310d6664144b76b5f68ff44f51e
出典メモuspto-grants-2012_08