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HRID 332837作成日:2026年10月26日
Sulfuric Acid → 5-(((1R,2S)-2-aminocyclohexyl)amino)-3-((5-fluoropyridin-3-yl)amino)pyrazine-2-carboxamide
https://huagongshe.com/reaction/332837
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | 5-Fluoro-3-pyridinamine | HCID 574450 | — |
| 反応物 | Binap, (A+-)- | HCID 634876 | — |
| 反応物 | HCID 86685625 | HCID 86685625 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Trifluoroacetic acid | HCID 6422 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 5-(((1R,2S)-2-aminocyclohexyl)amino)-3-((5-fluoropyridin-3-yl)amino)pyrazine-2-carboxamide | HCID 86685628 | 85.8% |
反応手順
The mixture of tert-tutyl ((1S,2R)-2-((6-chloro-5-cyanopyrazin-2-yl)amino)cyclohexyl)carbamate (100 mg, 0.28 mmol), 3-fluoro-5-aminopyridine (60 mg, 0.56 mmol), powder cesium carbonate (360 mg, 1.12 mmol), BINAP (37 mg, 0.06 mmol), Pd(OAc)2 (14 mg, 0.06 mmol) in 20 mL dioxane was degassed with argon stream. It was stirred in argon atmosphere at 110° C. for 2 h. The mixture was cooled, diluted with 100 mL EtOAc, vigorously stirred, and filtered through celite. The filtrate was concentrated and subjected to silica flash column with 0-60% EtOAc in hexane to isolate the coupling product. It was then stirred in 6 mL TFA and 1 mL conc. H2SO4 at 80° C. for 30 m. It was cooled in ice bath, diluted with water, filtered, and subjected to reverse phase preparative HPLC to isolate the title compound (83 mg). MS found for C16H20FN7O as (M+H)+ 346.5. UV: λ=259, 301 nm. 1H NMR: (CD3OD) δ 9.04 (1H, m), 8.57 (1H, m), 8.40 (1H, m), 7.73 (1H, s), 4.49 (1H, m), 3.74 (1H, m), 1.96-1.60 (8H, m) ppm.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08877760B2 |
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| 出典データセット | uspto-grants-2014_11 |
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| ORD ID | ord-29df8ee851fc429f83591399850729bf |
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| 出典メモ | uspto-grants-2014_11 |
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