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HRID 335992作成日:2026年10月24日
Benzeneethanamine, alpha-methyl-, phosphate (1:1) → (S)-7-(2-fluoropyridin-3-yl)-3-(pyrimidin-2-yl)-5'H-spiro[chromeno[2,3-b]pyridine-5,4'-thiazol]-2'-amine
https://huagongshe.com/ja/reaction/335992
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzeneethanamine, alpha-methyl-, phosphate (1:1) | HCID 62885 | — |
| 反応物 | 2-(Tributylstannyl)pyrimidine | HCID 2763251 | — |
| 反応物 | (S)-3-bromo-7-(2-fluoropyridin-3-yl)-5'H-spiro[chromeno[2,3-b]pyridine-5,4'-thiazol]-2'-amine | HCID 67438436 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | (S)-7-(2-fluoropyridin-3-yl)-3-(pyrimidin-2-yl)-5'H-spiro[chromeno[2,3-b]pyridine-5,4'-thiazol]-2'-amine | HCID 58466117 | 12% |
反応手順
A vial was charged with (S)-3-bromo-7-(2-fluoropyridin-3-yl)-5′H-spiro[chromeno[2,3-b]pyridine-5,4′-thiazol]-2′-amine (100 mg, 0.23 mmol), AmPhos (15.97 mg, 0.023 mmol), 2-(tributylstannyl)pyrimidine (333 mg, 0.90 mmol) and dioxane (1.50 mL). The vial was purged with Ar (g), sealed, and heated to 100° C. overnight. After cooling to rt, crude was diluted with MeOH (3 mL) and purified with reverse phase HPLC. Fractions containing product were washed with saturated aq. NaHCO3 (15 mL) and extracted with ethyl acetate (1×100 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo to provide a white solid, (S)-7-(2-fluoropyridin-3-yl)-3-(pyrimidin-2-yl)-5′H-spiro[chromeno[2,3-b]pyridine-5,4′-thiazol]-2′-amine (12 mg, 0.027 mmol, 12% yield). MS m/z=443.0 [M+H]+. Calc'd for C23H15FN6OS: 442.47.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08883782B2 |
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| 出典データセット | uspto-grants-2014_11 |
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| ORD ID | ord-70fd3fccf6804686aae1e94a19690e67 |
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| 出典メモ | uspto-grants-2014_11 |
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