関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | 2-Amino-6-methylpyridine | HCID 15765 | — |
| 反応物 | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| 反応物 | 8-Chloro-(1,7)naphthyridine | HCID 12342712 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | (6-Methyl-pyridin-2-yl)-[1,7]naphthyridin-8-yl-amine | HCID 16118550 | — |
反応手順
8-Chloro-[1,7]naphthyridine (Example A) (0.2 g, 1.2 mmol) and 2-amino-6-methylpyridine (0.13 g, 1.2 mmol) were dissolved in 8 ml dry dioxane. 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (145 mg, 0.24 mmol), cesium carbonate (0.63 g, 1.95 mmol) and tri(dibenzylideneacetone)dipalladium chloroform complex (0.13 g, 0.12 mmol) were added and the reaction mixture was stirred under microwave irradiation for 50 minutes at 150° C. The reaction mixture was then evaporated and purified by flash chromatography on silica gel (heptane/ethyl acetate 95:5->70:30 gradient). The desired product was obtained as a light yellow solid (98 mg, 34%),
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07511055B2 |
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| 出典データセット | uspto-grants-2009_03 |
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| ORD ID | ord-5937f0fba58341699293691ccde86743 |
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| 出典メモ | uspto-grants-2009_03 |
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