関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | 3-(4-Tert-butylphenyl)-1-[(2-chloropyridin-4-yl)methyl]-5,5-dimethylimidazolidine-2,4-dione | HCID 57625971 | — |
| 反応物 | (9,9-dimethyl-9H-xanthene-3,6-diyl)bis(diphenylphosphine) | HCID 86628973 | — |
| 反応物 | HCID 178507770 | HCID 178507770 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | HCID 178440998 | HCID 178440998 | 5.9% |
反応手順
To a solution of 0.5 g of 3-(4-tert-butylphenyl)-1-[(2-chloropyridin-4-yl)methyl]-5,5-dimethylimidazolidine-2,4-dione obtained in stage a) of Example 7 in 15 mL of dioxane are successively added, under argon, 285 mg of 5-amino-2-hydroxypyridine, 1.6 g of caesium carbonate, 90 mg of (9,9-dimethyl-9H-xanthene-3,6-diyl)bis(diphenylphosphine) [xantphos] and 29 mg of palladium diacetate. The reaction mixture is heated at 100° C. for 1 hour, filtered and concentrated under reduced pressure. The residue is successively purified by chromatography on a column of silica, eluting with a mixture of dichloromethane and methanol (95/5 by volume) followed by HPLC (gradient: water/acetonitrile containing 0.1% formic acid) to give 35 mg of 3-(4-tert-butylphenyl)-1-({2-[(6-hydroxypyridin-3-yl)amino]pyridin-4-yl}methyl)-5,5-dimethylimidazolidine-2,4-dione, the characteristics of which are as follows:
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07935819B2 |
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| 出典データセット | uspto-grants-2011_05 |
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| ORD ID | ord-8f523719e8d44afa9a05adf4078a6cb8 |
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| 出典メモ | uspto-grants-2011_05 |
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