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HRID 1516383作成日:2026年10月26日
Sodium Carbonate → 5-(3,4-Dichloro-phenyl)-N-((1S,2R)-2-hydroxy-cyclohexyl)-6-(2,2,2-trifluoro-ethoxy)-nicotinamide
https://huagongshe.com/reaction/1516383
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 3,4-Dichlorobenzeneboronic acid | HCID 2734330 | — |
| 反応物 | 5-Bromo-N-((1S,2R)-2-hydroxy-cyclohexyl)-6-(2,2,2-trifluoro-ethoxy)-nicotinamide | HCID 69812295 | — |
| 触媒 | HCID 178418807 | HCID 178418807 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 5-(3,4-Dichloro-phenyl)-N-((1S,2R)-2-hydroxy-cyclohexyl)-6-(2,2,2-trifluoro-ethoxy)-nicotinamide | HCID 50939054 | 67.8% |
反応手順
5-Bromo-N-((1S,2R)-2-hydroxy-cyclohexyl)-6-(2,2,2-trifluoro-ethoxy)-nicotinamide (42.0 g, 106 mmol) was dissolved in toluene (1900 mL) and DMF (100 mL). To this solution was added with stirring [1,1′-bis(diphenylphosphino)ferrocene]-dichloropalladium(II) CH2Cl2 (0.9 g, 1.06 mmol), 3,4-dichlorophenylboronic acid (20.2 g, 106 mmol) and sodium carbonate solution (2M, 106 mL). This mixture was heated to 90° C. for 2 h, cooled to room temperature and partitioned between ethyl acetate (1000 mL) and water (2000 mL), the water phase was separated, extracted twice more with ethyl acetate (2×1000 mL) and the organic phases were washed once with water and once with brine (1000 mL each). Organic phases were pooled, dried with MgSO4 and the volatiles removed in vacuo. The residue was dissolved in diethyl ether (500 mL) and filtered through diatomaceous earth. The title compound precipitated when n-heptane (500 mL) was added drop wise to the diethyl ether solution, was filtered off and dried in vacuo to give 33.3 g the title compound as an off-white solid; MS 463.079 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08227491B2 |
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| 出典データセット | uspto-grants-2012_07 |
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| ORD ID | ord-b0b4e41d5bd7418f8102e29af9df4bf5 |
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| 出典メモ | uspto-grants-2012_07 |
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