関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Methylpiperazine | HCID 53167 | — |
| 反応物 | 2-Chloro-4-iodopyridine | HCID 1516511 | — |
| 反応物 | Sodium t-butoxide | HCID 23676156 | — |
| 触媒 | Dichloro[1,1'-bis(di-tert-butylphosphino)ferrocene]palladium(II) | HCID 53384307 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 1-(2-Chloropyridin-4-YL)-4-methylpiperazine | HCID 72218899 | 77% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08242116B2 |
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| 出典データセット | uspto-grants-2012_08 |
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| ORD ID | ord-36642310d6664144b76b5f68ff44f51e |
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| 出典メモ | uspto-grants-2012_08 |
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