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HRID 1621388作成日:2026年10月27日
4-Chloro-6-methyl-1,3,5-triazin-2-amine → 4-(2-Fluoro-5-methylpyridin-3-yl)-6-methyl-1,3,5-triazin-2-amine
https://huagongshe.com/reaction/1621388
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 4-Chloro-6-methyl-1,3,5-triazin-2-amine | HCID 30591 | — |
| 反応物 | 1,4-Dioxane | HCID 31275 | — |
| 反応物 | Potassium Acetate | HCID 517044 | — |
| 反応物 | 2-Fluoro-5-methylpyridine-3-boronic acid | HCID 44754858 | — |
| 触媒 | Bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) | HCID 11714597 | — |
| 生成物 | 4-(2-Fluoro-5-methylpyridin-3-yl)-6-methyl-1,3,5-triazin-2-amine | HCID 60154718 | 41% |
反応手順
1,4-Dioxane (3.00 mL, 8.5 mmol) was added to a mixture of bis(di-tert-butyl (4-dimethylaminophenyl)phosphine)dichloropalladium(II) (Aldrich, St. Louis, Mo.) (0.27 g, 0.43 mmol), 2-fluoro-5-methylpyridin-3-ylboronic acid (1.6 g, 10 mmol), 4-chloro-6-methyl-1,3,5-triazin-2-amine (1.24 g, 8.5 mmol) and potassium acetate (2.5 g, 26 mmol) and the mixture was sealed and heated at 120° C. for 30 min under microwave irradiation. After cooling, the mixture was passed through a short plug of Celite® (diatomaceous earth). The filter cake was washed with DCM (3×20 mL). The combined organic phases were concentrated. Flash column chromatographic purification (short column, SiO2, pure DCM to 5% MeOH in DCM) provided 4-(2-fluoro-5-methylpyridin-3-yl)-6-methyl-1,3,5-triazin-2-amine (0.76, 41%) as a white solid which was used for the next step. LCMS (API-ES) m/z 220 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08772480B2 |
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| 出典データセット | uspto-grants-2014_07 |
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| ORD ID | ord-775a6bcf56494f58bf8e9eb74a7a2fbe |
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| 出典メモ | uspto-grants-2014_07 |
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