関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Fluoroaniline | HCID 9731 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 2-Chloro-6-[3-(trifluoromethyl)phenoxy]pyrazine | HCID 21266842 | — |
| 触媒 | (+/-)-1-[2-(Diphenylphosphino)ferrocenyl]ethyl-di-tert-butylphosphine | HCID 76007372 | — |
| 触媒 | HCID 178418476 | HCID 178418476 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | N-(4-Fluorophenyl)-6-[3-(trifluoromethyl)phenoxy]pyrazine-2-carboxamide | HCID 21266841 | 65.3% |
反応手順
Analogously to Example 3, 25 mmol of 2-chloro-6-[3-(trifluoromethyl)phenoxy]pyrazine (prepared according to U.S. Pat. No. 4,254,125, Example 21), 27.5 mmol of 4-fluoroaniline, 2.92 g (27.5 mmol) of sodium carbonate, 17.5 mg (25 μmol) of dichlorobis(triphenylphosphine)palladium(II) and 0.31 g (0.75 mmol) of (±)-1-[2-(diphenylphosphino)-ferrocenyl]ethyl-di-tert-butylphosphine in 25 ml of xylene were reacted under a CO pressure of 17 bar at 120° C. for 21 hours. The composition of the dissolved products in the xylene phase was determined by GC. 65.3 percent of the title compound (amide) and 34.7 percent of by-product (secondary amine) were found. The amide was isolated by column chromatography and purified. Data concerning the title product was:
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05922870 |
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| 出典データセット | uspto-grants-1999_07 |
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| ORD ID | ord-6430dfcc27fc4d51822ec38a44870022 |
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| 出典メモ | uspto-grants-1999_07 |
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