関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dichloromethane | HCID 6344 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 5-Bromopyridine-2-carbonitrile | HCID 817154 | — |
| 反応物 | 2-Cyclohexylvinyl boronic acid | HCID 4185149 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | (E)-5-(2-Cyclohexylvinyl)-pyridine-2-carbonitrile | HCID 58495465 | 76% |
反応手順
Combine a mixture of 5-bromo-2-cyano-pyridine (2 g, 10.93 mmol), 2-cyclohexylvinyl boronic acid (2.52 g, 16.39 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) complex with DCM (446 mg, 0.546 mmol) and 2M aqueous Na2CO3 (18.2 mL, 36.07 mmol) in 1,4-dioxane (110 mL). Purge with nitrogen and heat at 90° C. overnight. Cool the reaction to room temperature and partition between EtOAc and water. Separate the aqueous phase and extract with EtOAc. Dry the combined organic extracts over MgSO4, filter and concentrate in vacuo. Purify by chromatography on silica gel (120 g, pre-packed cartridge) eluting stepwise with hexane/EtOAc (1:0 over 5 min, 49:1 over 5 min and 19:1 over 5 min; 50 mL/min) to obtain the desired intermediate (1.76 g, 76%). MS (APCI+) m/z: 213 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08680091B2 |
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| 出典データセット | uspto-grants-2014_03 |
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| ORD ID | ord-01ff898b45c445bcab9f091c7aabacf8 |
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| 出典メモ | uspto-grants-2014_03 |
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